Canonical Allele Identifier: CA1618519751

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944657T= , CM000668.2:g.29944657T=	GRCh38
NC_000006.11:g.29912434T= , CM000668.1:g.29912434T=	GRCh37
NC_000006.10:g.30020413T=	NCBI36
NG_029217.2:g.7193T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+260T=	ENSP00000492789.2:n.895+260T=
ENST00000706892.1:n.2009T=
ENST00000706893.1:c.1064+23T=	ENSP00000516609.1:n.1064+23T=
ENST00000706894.1:c.1012+41T=	ENSP00000516610.1:n.1012+41T=
ENST00000706895.1:n.1431T=
ENST00000706896.1:n.1907T=
ENST00000706897.1:n.1329T=
ENST00000706898.1:c.1030+23T=	ENSP00000516611.1:n.1030+23T=
ENST00000706899.1:n.1866+41T=
ENST00000706900.1:c.928+41T=	ENSP00000516617.1:n.928+41T=
ENST00000706901.1:c.1012+41T=	ENSP00000516612.1:n.1012+41T=
ENST00000706902.1:c.1012+41T=	ENSP00000516613.1:n.1012+41T=
ENST00000706903.1:c.1012+41T=	ENSP00000516614.1:n.1012+41T=
ENST00000706904.1:c.1012+41T=	ENSP00000516615.1:n.1012+41T=
ENST00000706905.1:c.1012+41T=	ENSP00000516616.1:n.1012+41T=
ENST00000376809.10:c.1012+41T= MANE Select	ENSP00000366005.5:n.1012+41T=
ENST00000638375.1:c.895+260T=	ENSP00000492789.1:n.895+260T=
ENST00000376802.2:c.895+260T=	ENSP00000365998.2:n.895+260T=
ENST00000376806.9:c.1030+23T=	ENSP00000366002.5:n.1030+23T=
ENST00000376809.9:c.1012+41T=	ENSP00000366005.5:n.1012+41T=
ENST00000396634.5:c.1012+41T=	ENSP00000379873.1:n.1012+41T=
ENST00000461903.1:n.1271+23T=
ENST00000479320.5:n.1253+41T=
ENST00000495183.5:n.1255+41T=
ENST00000496081.5:n.870T=
NM_002116.7:c.1012+41T=	NP_002107.3:n.1012+41T=
NM_002116.8:c.1012+41T= MANE Select	NP_002107.3:n.1012+41T=