Canonical Allele Identifier: CA1618521007

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945684G= , CM000668.2:g.29945684G=	GRCh38
NC_000006.11:g.29913461G= , CM000668.1:g.29913461G=	GRCh37
NC_000006.10:g.30021440G=	NCBI36
NG_029217.2:g.8220G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1210G=	ENSP00000492789.2:n.1210G=
ENST00000706892.1:n.3036G=
ENST00000706893.1:c.*311G=	ENSP00000516609.1:n.*311G=
ENST00000706894.1:c.*311G=	ENSP00000516610.1:n.*311G=
ENST00000706895.1:n.2316G=
ENST00000706896.1:n.2623G=
ENST00000706897.1:n.2045G=
ENST00000706898.1:c.*229G=	ENSP00000516611.1:n.*229G=
ENST00000706899.1:n.2181G=
ENST00000706900.1:c.*229G=	ENSP00000516617.1:n.*229G=
ENST00000706901.1:c.*229G=	ENSP00000516612.1:n.*229G=
ENST00000706902.1:c.1093+403G=	ENSP00000516613.1:n.1093+403G=
ENST00000706903.1:c.*124+105G=	ENSP00000516614.1:n.*124+105G=
ENST00000706904.1:c.1093+403G=	ENSP00000516615.1:n.1093+403G=
ENST00000706905.1:c.*229G=	ENSP00000516616.1:n.*229G=
ENST00000376809.10:c.*229G= MANE Select	ENSP00000366005.5:n.*229G=
ENST00000376802.2:c.*229G=	ENSP00000365998.2:n.*229G=
ENST00000376806.9:c.*229G=	ENSP00000366002.5:n.*229G=
ENST00000376809.9:c.*229G=	ENSP00000366005.5:n.*229G=
ENST00000396634.5:c.*229G=	ENSP00000379873.1:n.*229G=
ENST00000495183.5:n.1566G=
ENST00000496081.5:n.1586G=
NM_002116.7:c.*229G=	NP_002107.3:n.*229G=
NM_002116.8:c.*229G= MANE Select	NP_002107.3:n.*229G=