Canonical Allele Identifier: CA1087350021
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v3: 6-29945368-T-C
gnomAD v4: 6-29945368-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945368T>C , CM000668.2:g.29945368T>C GRCh38
NC_000006.11:g.29913145T>C , CM000668.1:g.29913145T>C GRCh37
NC_000006.10:g.30021124T>C NCBI36
NG_029217.2:g.7904T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.977-83T>C ENSP00000492789.2:n.977-83T>C
ENST00000706892.1:n.2720T>C
ENST00000706893.1:c.*78-83T>C ENSP00000516609.1:n.*78-83T>C
ENST00000706894.1:c.1180T>C ENSP00000516610.1:p.Tyr394His
ENST00000706895.1:n.2000T>C
ENST00000706896.1:n.2390-83T>C
ENST00000706897.1:n.1812-83T>C
ENST00000706898.1:c.1112-83T>C ENSP00000516611.1:n.1112-83T>C
ENST00000706899.1:n.1948-83T>C
ENST00000706900.1:c.1010-83T>C ENSP00000516617.1:n.1010-83T>C
ENST00000706901.1:c.1094-83T>C ENSP00000516612.1:n.1094-83T>C
ENST00000706902.1:c.1093+87T>C ENSP00000516613.1:n.1093+87T>C
ENST00000706903.1:c.1094-83T>C ENSP00000516614.1:n.1094-83T>C
ENST00000706904.1:c.1093+87T>C ENSP00000516615.1:n.1093+87T>C
ENST00000706905.1:c.1094-83T>C ENSP00000516616.1:n.1094-83T>C
ENST00000376809.10:c.1094-83T>C MANE Select ENSP00000366005.5:n.1094-83T>C
ENST00000376802.2:c.896-83T>C ENSP00000365998.2:n.896-83T>C
ENST00000376806.9:c.1112-83T>C ENSP00000366002.5:n.1112-83T>C
ENST00000376809.9:c.1094-83T>C ENSP00000366005.5:n.1094-83T>C
ENST00000396634.5:c.1094-83T>C ENSP00000379873.1:n.1094-83T>C
ENST00000495183.5:n.1333-83T>C
ENST00000496081.5:n.1353-83T>C
NM_002116.7:c.1094-83T>C NP_002107.3:n.1094-83T>C
NM_002116.8:c.1094-83T>C MANE Select NP_002107.3:n.1094-83T>C