Canonical Allele Identifier: CA1618519993

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944823T= , CM000668.2:g.29944823T=	GRCh38
NC_000006.11:g.29912600T= , CM000668.1:g.29912600T=	GRCh37
NC_000006.10:g.30020579T=	NCBI36
NG_029217.2:g.7359T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.896-236T=	ENSP00000492789.2:n.896-236T=
ENST00000706892.1:n.2175T=
ENST00000706893.1:c.1064+189T=	ENSP00000516609.1:n.1064+189T=
ENST00000706894.1:c.1012+207T=	ENSP00000516610.1:n.1012+207T=
ENST00000706895.1:n.1597T=
ENST00000706896.1:n.2073T=
ENST00000706897.1:n.1495T=
ENST00000706898.1:c.1030+189T=	ENSP00000516611.1:n.1030+189T=
ENST00000706899.1:n.1866+207T=
ENST00000706900.1:c.928+207T=	ENSP00000516617.1:n.928+207T=
ENST00000706901.1:c.1012+207T=	ENSP00000516612.1:n.1012+207T=
ENST00000706902.1:c.1012+207T=	ENSP00000516613.1:n.1012+207T=
ENST00000706903.1:c.1012+207T=	ENSP00000516614.1:n.1012+207T=
ENST00000706904.1:c.1012+207T=	ENSP00000516615.1:n.1012+207T=
ENST00000706905.1:c.1012+207T=	ENSP00000516616.1:n.1012+207T=
ENST00000376809.10:c.1012+207T= MANE Select	ENSP00000366005.5:n.1012+207T=
ENST00000638375.1:c.896-236T=	ENSP00000492789.1:n.896-236T=
ENST00000376802.2:c.895+426T=	ENSP00000365998.2:n.895+426T=
ENST00000376806.9:c.1030+189T=	ENSP00000366002.5:n.1030+189T=
ENST00000376809.9:c.1012+207T=	ENSP00000366005.5:n.1012+207T=
ENST00000396634.5:c.1012+207T=	ENSP00000379873.1:n.1012+207T=
ENST00000461903.1:n.1271+189T=
ENST00000479320.5:n.1253+207T=
ENST00000495183.5:n.1255+207T=
ENST00000496081.5:n.1036T=
NM_002116.7:c.1012+207T=	NP_002107.3:n.1012+207T=
NM_002116.8:c.1012+207T= MANE Select	NP_002107.3:n.1012+207T=