Canonical Allele Identifier: CA2594382445
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1771618072
gnomAD v3: 6-29945829-T-C
gnomAD v4: 6-29945829-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945829T>C , CM000668.2:g.29945829T>C GRCh38
NC_000006.11:g.29913606T>C , CM000668.1:g.29913606T>C GRCh37
NC_000006.10:g.30021585T>C NCBI36
NG_029217.2:g.8365T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1355T>C ENSP00000492789.2:n.1355T>C
ENST00000706896.1:n.2768T>C
ENST00000706897.1:n.2190T>C
ENST00000706898.1:c.*374T>C ENSP00000516611.1:n.*374T>C
ENST00000706899.1:n.2326T>C
ENST00000706900.1:c.*374T>C ENSP00000516617.1:n.*374T>C
ENST00000706901.1:c.*374T>C ENSP00000516612.1:n.*374T>C
ENST00000706902.1:c.1093+548T>C ENSP00000516613.1:n.1093+548T>C
ENST00000706903.1:c.*124+250T>C ENSP00000516614.1:n.*124+250T>C
ENST00000706904.1:c.1093+548T>C ENSP00000516615.1:n.1093+548T>C
ENST00000706905.1:c.*374T>C ENSP00000516616.1:n.*374T>C
ENST00000376809.10:c.*374T>C MANE Select ENSP00000366005.5:n.*374T>C
ENST00000376802.2:c.*374T>C ENSP00000365998.2:n.*374T>C
ENST00000376806.9:c.*374T>C ENSP00000366002.5:n.*374T>C
ENST00000376809.9:c.*374T>C ENSP00000366005.5:n.*374T>C
ENST00000396634.5:c.*374T>C ENSP00000379873.1:n.*374T>C
ENST00000495183.5:n.1711T>C
ENST00000496081.5:n.1731T>C
NM_002116.7:c.*374T>C NP_002107.3:n.*374T>C
NM_002116.8:c.*374T>C MANE Select NP_002107.3:n.*374T>C