Canonical Allele Identifier: CA1618519859

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944716G= , CM000668.2:g.29944716G=	GRCh38
NC_000006.11:g.29912493G= , CM000668.1:g.29912493G=	GRCh37
NC_000006.10:g.30020472G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+319G=	ENSP00000492789.2:n.895+319G=
ENST00000706892.1:n.2068G=
ENST00000706893.1:c.1064+82G=	ENSP00000516609.1:n.1064+82G=
ENST00000706894.1:c.1012+100G=	ENSP00000516610.1:n.1012+100G=
ENST00000706895.1:n.1490G=
ENST00000706896.1:n.1966G=
ENST00000706897.1:n.1388G=
ENST00000706898.1:c.1030+82G=	ENSP00000516611.1:n.1030+82G=
ENST00000706899.1:n.1866+100G=
ENST00000706900.1:c.928+100G=	ENSP00000516617.1:n.928+100G=
ENST00000706901.1:c.1012+100G=	ENSP00000516612.1:n.1012+100G=
ENST00000706902.1:c.1012+100G=	ENSP00000516613.1:n.1012+100G=
ENST00000706903.1:c.1012+100G=	ENSP00000516614.1:n.1012+100G=
ENST00000706904.1:c.1012+100G=	ENSP00000516615.1:n.1012+100G=
ENST00000706905.1:c.1012+100G=	ENSP00000516616.1:n.1012+100G=
ENST00000376809.10:c.1012+100G= MANE Select	ENSP00000366005.5:n.1012+100G=
ENST00000638375.1:c.895+319G=	ENSP00000492789.1:n.895+319G=
ENST00000376802.2:c.895+319G=	ENSP00000365998.2:n.895+319G=
ENST00000376806.9:c.1030+82G=	ENSP00000366002.5:n.1030+82G=
ENST00000376809.9:c.1012+100G=	ENSP00000366005.5:n.1012+100G=
ENST00000396634.5:c.1012+100G=	ENSP00000379873.1:n.1012+100G=
ENST00000461903.1:n.1271+82G=
ENST00000479320.5:n.1253+100G=
ENST00000495183.5:n.1255+100G=
ENST00000496081.5:n.929G=
NM_002116.7:c.1012+100G=	NP_002107.3:n.1012+100G=
NM_002116.8:c.1012+100G= MANE Select	NP_002107.3:n.1012+100G=