Canonical Allele Identifier: CA1618520625
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945396T= , CM000668.2:g.29945396T= GRCh38
NC_000006.11:g.29913173T= , CM000668.1:g.29913173T= GRCh37
NC_000006.10:g.30021152T= NCBI36
NG_029217.2:g.7932T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.977-55T= ENSP00000492789.2:n.977-55T=
ENST00000706892.1:n.2748T=
ENST00000706893.1:c.*78-55T= ENSP00000516609.1:n.*78-55T=
ENST00000706894.1:c.*23T= ENSP00000516610.1:n.*23T=
ENST00000706895.1:n.2028T=
ENST00000706896.1:n.2390-55T=
ENST00000706897.1:n.1812-55T=
ENST00000706898.1:c.1112-55T= ENSP00000516611.1:n.1112-55T=
ENST00000706899.1:n.1948-55T=
ENST00000706900.1:c.1010-55T= ENSP00000516617.1:n.1010-55T=
ENST00000706901.1:c.1094-55T= ENSP00000516612.1:n.1094-55T=
ENST00000706902.1:c.1093+115T= ENSP00000516613.1:n.1093+115T=
ENST00000706903.1:c.1094-55T= ENSP00000516614.1:n.1094-55T=
ENST00000706904.1:c.1093+115T= ENSP00000516615.1:n.1093+115T=
ENST00000706905.1:c.1094-55T= ENSP00000516616.1:n.1094-55T=
ENST00000376809.10:c.1094-55T= MANE Select ENSP00000366005.5:n.1094-55T=
ENST00000376802.2:c.896-55T= ENSP00000365998.2:n.896-55T=
ENST00000376806.9:c.1112-55T= ENSP00000366002.5:n.1112-55T=
ENST00000376809.9:c.1094-55T= ENSP00000366005.5:n.1094-55T=
ENST00000396634.5:c.1094-55T= ENSP00000379873.1:n.1094-55T=
ENST00000495183.5:n.1333-55T=
ENST00000496081.5:n.1353-55T=
NM_002116.7:c.1094-55T= NP_002107.3:n.1094-55T=
NM_002116.8:c.1094-55T= MANE Select NP_002107.3:n.1094-55T=