Canonical Allele Identifier: CA1618521045

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945724C= , CM000668.2:g.29945724C=	GRCh38
NC_000006.11:g.29913501C= , CM000668.1:g.29913501C=	GRCh37
NC_000006.10:g.30021480C=	NCBI36
NG_029217.2:g.8260C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1250C=	ENSP00000492789.2:n.1250C=
ENST00000706893.1:c.*351C=	ENSP00000516609.1:n.*351C=
ENST00000706894.1:c.*351C=	ENSP00000516610.1:n.*351C=
ENST00000706895.1:n.2356C=
ENST00000706896.1:n.2663C=
ENST00000706897.1:n.2085C=
ENST00000706898.1:c.*269C=	ENSP00000516611.1:n.*269C=
ENST00000706899.1:n.2221C=
ENST00000706900.1:c.*269C=	ENSP00000516617.1:n.*269C=
ENST00000706901.1:c.*269C=	ENSP00000516612.1:n.*269C=
ENST00000706902.1:c.1093+443C=	ENSP00000516613.1:n.1093+443C=
ENST00000706903.1:c.*124+145C=	ENSP00000516614.1:n.*124+145C=
ENST00000706904.1:c.1093+443C=	ENSP00000516615.1:n.1093+443C=
ENST00000706905.1:c.*269C=	ENSP00000516616.1:n.*269C=
ENST00000376809.10:c.*269C= MANE Select	ENSP00000366005.5:n.*269C=
ENST00000376802.2:c.*269C=	ENSP00000365998.2:n.*269C=
ENST00000376806.9:c.*269C=	ENSP00000366002.5:n.*269C=
ENST00000376809.9:c.*269C=	ENSP00000366005.5:n.*269C=
ENST00000396634.5:c.*269C=	ENSP00000379873.1:n.*269C=
ENST00000495183.5:n.1606C=
ENST00000496081.5:n.1626C=
NM_002116.7:c.*269C=	NP_002107.3:n.*269C=
NM_002116.8:c.*269C= MANE Select	NP_002107.3:n.*269C=