This module comprises all classical HLA alleles registered on the IMGT/HLA Database
as of Release 3.7.0 and the
number of times that each allele has been reported to different databases such as the
Allele Frequency Net Database (AFND), the
National Marrow Donor Program (NMDP) in the US
as of Release 3.5.0 and other individual laboratories.
The aim of this page is that a user can identify HLA rare alleles by filtering the total times an HLA allele has been reported
to these Databases.
E.g. Cells < 3, Groups < 3, Pops < 2, NMDP < 2, Labs < 2.
This project has been included in the 16th International HLA and Immunogenetics Worskhop (IHWS) in Liverpool (28-30 March 2012).
Previous results were published on Tissue Antigens 2009 74:480-485 [See abstract].
If an allele that we consider to be rare has been typed in your laboratory, please report it by clicking on the "
" image beside the allele.
Basic information will be required to complete your submissions. Your contribution is vital to confirm the number of rare alleles!.
Click here to see the list of current contributors.
Special announcement: All contributors that have sent data will be included as participants of the 16th IHWS.
Deadline to submit your data has been extended to 15th April 2012. You can still submit your data after that date but it will not be shown in the conference.
New tool: Rare Allele Detector
To facilitate the analysis of large datasets (i.e. 1000 individuals typed) the Rare Allele Detector tool has been incorporated to the AFND website.
This tool simplifies the detection of alleles which are considered to be very rare, rare or frequent. Click here to try this tool.
Rare alleles can be filtered according to how many times it is since they were first sequenced. Please select your criteria by using different options and click "Search".
| IMGT/HLA | Allele Frequencies Website | IMGT/HLA (See details) |
NMDP (See details) |
Other Labs (See details) |
Total (...) |
ASHI (...) |
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|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Allele | Pops with allele in website | See lower resolution | See sequences identical over exons 2 + 3 ¹ | Allele initially sequenced in population | Year | Sequence confirmed | Cells | Groups | Length | Total | AFA | API | CAU | HIS | NAM | OTH | Total | BLA | CAU | MES | HIS | OTH | ||||
| 1 | A*01:01:01:01 | 4 | A*01:01, A*01:01:01 | A*01:01:01:02N, A*01:04N, A*01:22N, A*01:32, A*01:34N, A*01:37, A*01:45, A*01:56N, A*01:81 | Caucasoid - England, Europe; Caucasoid - South Africa, Southern Africa | 1989 | Confirmed | 7 | 7 | Full | - | NA | >4 | C/WD US | ||||||||||||
| 2 | A*01:01:01:02N
| 0 | A*01:01, A*01:01:01 | A*01:01:01:01, A*01:04N, A*01:22N, A*01:32, A*01:34N, A*01:37, A*01:45, A*01:56N, A*01:81 | Caucasoid - Spain, Europe | 2005 | Unconfirmed | 1 | 1 | Full | - | 1 | 1 | 2 | ||||||||||||
| 3 | A*01:01:02
| 0 | A*01:01 | Mixed - American Indian/Caucasoid | 2000 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | ||||||||||||||
| 4 | A*01:01:03
| 0 | A*01:01 | Unknown | 2004 | Confirmed | 3 | 2 | Partial | - | - | 3 | ||||||||||||||
| 5 | A*01:01:04
| 0 | A*01:01 | Unknown | 2006 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | ||||||||||||||
| 6 | A*01:01:05
| 0 | A*01:01 | Caucasoid - Germany, Europe | 2007 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | ||||||||||||||
| 7 | A*01:01:06
| 0 | A*01:01 | 2009 | Confirmed | 3 | 1 | Partial | - | - | 3 | |||||||||||||||
| 8 | A*01:01:07
| 0 | A*01:01 | 2009 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 9 | A*01:01:08
| 0 | A*01:01 | 2009 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 10 | A*01:01:09
| 0 | A*01:01 | 2009 | Confirmed | 4 | 1 | Partial | - | - | 4 | |||||||||||||||
| 11 | A*01:01:10 | 0 | A*01:01 | 2009 | Confirmed | 19 | 1 | Partial | - | NA | >4 | |||||||||||||||
| 12 | A*01:01:11 | 0 | A*01:01 | 2009 | Confirmed | 10 | 1 | Partial | - | NA | >4 | |||||||||||||||
| 13 | A*01:01:12
| 0 | A*01:01 | 2009 | Confirmed | 2 | 1 | Partial | - | - | 2 | |||||||||||||||
| 14 | A*01:01:13
| 0 | A*01:01 | 2009 | Confirmed | 4 | 1 | Partial | - | - | 4 | |||||||||||||||
| 15 | A*01:01:14
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 16 | A*01:01:15
| 0 | A*01:01 | 2010 | Confirmed | 2 | 2 | Partial | - | - | 2 | |||||||||||||||
| 17 | A*01:01:16 | 0 | A*01:01 | 2010 | Confirmed | 6 | 2 | Partial | - | NA | >4 | |||||||||||||||
| 18 | A*01:01:17
| 0 | A*01:01 | 2010 | Confirmed | 4 | 1 | Partial | - | - | 4 | |||||||||||||||
| 19 | A*01:01:18
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 20 | A*01:01:19
| 0 | A*01:01 | 2010 | Confirmed | 2 | 1 | Partial | - | - | 2 | |||||||||||||||
| 21 | A*01:01:20
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 22 | A*01:01:21
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 23 | A*01:01:22
| 0 | A*01:01 | 2010 | Confirmed | 4 | 2 | Partial | - | - | 4 | |||||||||||||||
| 24 | A*01:01:23
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 25 | A*01:01:24
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 26 | A*01:01:25
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 27 | A*01:01:26
| 0 | A*01:01 | 2010 | Confirmed | 2 | 2 | Partial | - | - | 2 | |||||||||||||||
| 28 | A*01:01:27
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 29 | A*01:01:28
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
| 30 | A*01:01:29
| 0 | A*01:01 | 2010 | Unconfirmed | 1 | 1 | Partial | - | - | 1 | |||||||||||||||
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