Canonical Allele Identifier: CA1618521002

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945681T= , CM000668.2:g.29945681T=	GRCh38
NC_000006.11:g.29913458T= , CM000668.1:g.29913458T=	GRCh37
NC_000006.10:g.30021437T=	NCBI36
NG_029217.2:g.8217T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1207T=	ENSP00000492789.2:n.1207T=
ENST00000706892.1:n.3033T=
ENST00000706893.1:c.*308T=	ENSP00000516609.1:n.*308T=
ENST00000706894.1:c.*308T=	ENSP00000516610.1:n.*308T=
ENST00000706895.1:n.2313T=
ENST00000706896.1:n.2620T=
ENST00000706897.1:n.2042T=
ENST00000706898.1:c.*226T=	ENSP00000516611.1:n.*226T=
ENST00000706899.1:n.2178T=
ENST00000706900.1:c.*226T=	ENSP00000516617.1:n.*226T=
ENST00000706901.1:c.*226T=	ENSP00000516612.1:n.*226T=
ENST00000706902.1:c.1093+400T=	ENSP00000516613.1:n.1093+400T=
ENST00000706903.1:c.*124+102T=	ENSP00000516614.1:n.*124+102T=
ENST00000706904.1:c.1093+400T=	ENSP00000516615.1:n.1093+400T=
ENST00000706905.1:c.*226T=	ENSP00000516616.1:n.*226T=
ENST00000376809.10:c.*226T= MANE Select	ENSP00000366005.5:n.*226T=
ENST00000376802.2:c.*226T=	ENSP00000365998.2:n.*226T=
ENST00000376806.9:c.*226T=	ENSP00000366002.5:n.*226T=
ENST00000376809.9:c.*226T=	ENSP00000366005.5:n.*226T=
ENST00000396634.5:c.*226T=	ENSP00000379873.1:n.*226T=
ENST00000495183.5:n.1563T=
ENST00000496081.5:n.1583T=
NM_002116.7:c.*226T=	NP_002107.3:n.*226T=
NM_002116.8:c.*226T= MANE Select	NP_002107.3:n.*226T=