Canonical Allele Identifier: CA1618520477

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945281G= , CM000668.2:g.29945281G=	GRCh38
NC_000006.11:g.29913058G= , CM000668.1:g.29913058G=	GRCh37
NC_000006.10:g.30021037G=	NCBI36
NG_029217.2:g.7817G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976G=	ENSP00000492789.2:p.Val326=
ENST00000706892.1:n.2633G=
ENST00000706893.1:c.*77G=	ENSP00000516609.1:n.*77G=
ENST00000706894.1:c.1093G=	ENSP00000516610.1:p.Gly365=
ENST00000706895.1:n.1913G=
ENST00000706896.1:n.2389G=
ENST00000706897.1:n.1811G=
ENST00000706898.1:c.1111G=	ENSP00000516611.1:p.Val371=
ENST00000706899.1:n.1947G=
ENST00000706900.1:c.1009G=	ENSP00000516617.1:p.Val337=
ENST00000706901.1:c.1093G=	ENSP00000516612.1:p.Val365=
ENST00000706902.1:c.1093G=	ENSP00000516613.1:p.Glu365=
ENST00000706903.1:c.1093G=	ENSP00000516614.1:p.Val365=
ENST00000706904.1:c.1093G=	ENSP00000516615.1:p.Glu365=
ENST00000706905.1:c.1093G=	ENSP00000516616.1:p.Val365=
ENST00000376809.10:c.1093G= MANE Select	ENSP00000366005.5:p.Val365=
ENST00000376802.2:c.896-170G=	ENSP00000365998.2:n.896-170G=
ENST00000376806.9:c.1111G=	ENSP00000366002.5:p.Val371=
ENST00000376809.9:c.1093G=	ENSP00000366005.5:p.Val365=
ENST00000396634.5:c.1093G=	ENSP00000379873.1:p.Val365=
ENST00000461903.1:n.1352G=
ENST00000479320.5:n.1334G=
ENST00000495183.5:n.1332G=
ENST00000496081.5:n.1352G=
NM_002116.7:c.1093G=	NP_002107.3:p.Val365=
NM_002116.8:c.1093G= MANE Select	NP_002107.3:p.Val365=