Canonical Allele Identifier: CA1618519639

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944609G= , CM000668.2:g.29944609G=	GRCh38
NC_000006.11:g.29912386G= , CM000668.1:g.29912386G=	GRCh37
NC_000006.10:g.30020365G=	NCBI36
NG_029217.2:g.7145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+212G=	ENSP00000492789.2:n.895+212G=
ENST00000706892.1:n.1961G=
ENST00000706893.1:c.1039G=	ENSP00000516609.1:p.Glu347=
ENST00000706894.1:c.1005G=	ENSP00000516610.1:p.Lys335=
ENST00000706895.1:n.1383G=
ENST00000706896.1:n.1859G=
ENST00000706897.1:n.1281G=
ENST00000706898.1:c.1005G=	ENSP00000516611.1:p.Lys335=
ENST00000706899.1:n.1859G=
ENST00000706900.1:c.921G=	ENSP00000516617.1:p.Lys307=
ENST00000706901.1:c.1005G=	ENSP00000516612.1:p.Lys335=
ENST00000706902.1:c.1005G=	ENSP00000516613.1:p.Lys335=
ENST00000706903.1:c.1005G=	ENSP00000516614.1:p.Lys335=
ENST00000706904.1:c.1005G=	ENSP00000516615.1:p.Lys335=
ENST00000706905.1:c.1005G=	ENSP00000516616.1:p.Lys335=
ENST00000376809.10:c.1005G= MANE Select	ENSP00000366005.5:p.Lys335=
ENST00000638375.1:c.895+212G=	ENSP00000492789.1:n.895+212G=
ENST00000376802.2:c.895+212G=	ENSP00000365998.2:n.895+212G=
ENST00000376806.9:c.1005G=	ENSP00000366002.5:p.Lys335=
ENST00000376809.9:c.1005G=	ENSP00000366005.5:p.Lys335=
ENST00000396634.5:c.1005G=	ENSP00000379873.1:p.Lys335=
ENST00000461903.1:n.1246G=
ENST00000479320.5:n.1246G=
ENST00000495183.5:n.1248G=
ENST00000496081.5:n.822G=
NM_002116.7:c.1005G=	NP_002107.3:p.Lys335=
NM_002116.8:c.1005G= MANE Select	NP_002107.3:p.Lys335=