Canonical Allele Identifier: CA1618521105
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1582009356
gnomAD v4: 6-29945810-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945810A>G , CM000668.2:g.29945810A>G GRCh38
NC_000006.11:g.29913587A>G , CM000668.1:g.29913587A>G GRCh37
NC_000006.10:g.30021566A>G NCBI36
NG_029217.2:g.8346A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1336A>G ENSP00000492789.2:n.1336A>G
ENST00000706896.1:n.2749A>G
ENST00000706897.1:n.2171A>G
ENST00000706898.1:c.*355A>G ENSP00000516611.1:n.*355A>G
ENST00000706899.1:n.2307A>G
ENST00000706900.1:c.*355A>G ENSP00000516617.1:n.*355A>G
ENST00000706901.1:c.*355A>G ENSP00000516612.1:n.*355A>G
ENST00000706902.1:c.1093+529A>G ENSP00000516613.1:n.1093+529A>G
ENST00000706903.1:c.*124+231A>G ENSP00000516614.1:n.*124+231A>G
ENST00000706904.1:c.1093+529A>G ENSP00000516615.1:n.1093+529A>G
ENST00000706905.1:c.*355A>G ENSP00000516616.1:n.*355A>G
ENST00000376809.10:c.*355A>G MANE Select ENSP00000366005.5:n.*355A>G
ENST00000376802.2:c.*355A>G ENSP00000365998.2:n.*355A>G
ENST00000376806.9:c.*355A>G ENSP00000366002.5:n.*355A>G
ENST00000376809.9:c.*355A>G ENSP00000366005.5:n.*355A>G
ENST00000396634.5:c.*355A>G ENSP00000379873.1:n.*355A>G
ENST00000495183.5:n.1692A>G
ENST00000496081.5:n.1712A>G
NM_002116.7:c.*355A>G NP_002107.3:n.*355A>G
NM_002116.8:c.*355A>G MANE Select NP_002107.3:n.*355A>G