Canonical Allele Identifier: CA1618521059
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945742C= , CM000668.2:g.29945742C= GRCh38
NC_000006.11:g.29913519C= , CM000668.1:g.29913519C= GRCh37
NC_000006.10:g.30021498C= NCBI36
NG_029217.2:g.8278C=

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.1268C= ENSP00000492789.2:n.1268C=
ENST00000706894.1:c.*369C= ENSP00000516610.1:n.*369C=
ENST00000706895.1:n.2374C=
ENST00000706896.1:n.2681C=
ENST00000706897.1:n.2103C=
ENST00000706898.1:c.*287C= ENSP00000516611.1:n.*287C=
ENST00000706899.1:n.2239C=
ENST00000706900.1:c.*287C= ENSP00000516617.1:n.*287C=
ENST00000706901.1:c.*287C= ENSP00000516612.1:n.*287C=
ENST00000706902.1:c.1093+461C= ENSP00000516613.1:n.1093+461C=
ENST00000706903.1:c.*124+163C= ENSP00000516614.1:n.*124+163C=
ENST00000706904.1:c.1093+461C= ENSP00000516615.1:n.1093+461C=
ENST00000706905.1:c.*287C= ENSP00000516616.1:n.*287C=
ENST00000376809.10:c.*287C= MANE Select ENSP00000366005.5:n.*287C=
ENST00000376802.2:c.*287C= ENSP00000365998.2:n.*287C=
ENST00000376806.9:c.*287C= ENSP00000366002.5:n.*287C=
ENST00000376809.9:c.*287C= ENSP00000366005.5:n.*287C=
ENST00000396634.5:c.*287C= ENSP00000379873.1:n.*287C=
ENST00000495183.5:n.1624C=
ENST00000496081.5:n.1644C=
NM_002116.7:c.*287C= NP_002107.3:n.*287C=
NM_002116.8:c.*287C= MANE Select NP_002107.3:n.*287C=