Canonical Allele Identifier: CA1618519611

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944591C= , CM000668.2:g.29944591C=	GRCh38
NC_000006.11:g.29912368C= , CM000668.1:g.29912368C=	GRCh37
NC_000006.10:g.30020347C=	NCBI36
NG_029217.2:g.7127C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+194C=	ENSP00000492789.2:n.895+194C=
ENST00000706892.1:n.1943C=
ENST00000706893.1:c.1021C=	ENSP00000516609.1:p.Arg341=
ENST00000706894.1:c.987C=	ENSP00000516610.1:p.Ala329=
ENST00000706895.1:n.1365C=
ENST00000706896.1:n.1841C=
ENST00000706897.1:n.1263C=
ENST00000706898.1:c.987C=	ENSP00000516611.1:p.Ala329=
ENST00000706899.1:n.1841C=
ENST00000706900.1:c.903C=	ENSP00000516617.1:p.Ala301=
ENST00000706901.1:c.987C=	ENSP00000516612.1:p.Ala329=
ENST00000706902.1:c.987C=	ENSP00000516613.1:p.Ala329=
ENST00000706903.1:c.987C=	ENSP00000516614.1:p.Ala329=
ENST00000706904.1:c.987C=	ENSP00000516615.1:p.Ala329=
ENST00000706905.1:c.987C=	ENSP00000516616.1:p.Ala329=
ENST00000376809.10:c.987C= MANE Select	ENSP00000366005.5:p.Ala329=
ENST00000638375.1:c.895+194C=	ENSP00000492789.1:n.895+194C=
ENST00000376802.2:c.895+194C=	ENSP00000365998.2:n.895+194C=
ENST00000376806.9:c.987C=	ENSP00000366002.5:p.Ala329=
ENST00000376809.9:c.987C=	ENSP00000366005.5:p.Ala329=
ENST00000396634.5:c.987C=	ENSP00000379873.1:p.Ala329=
ENST00000461903.1:n.1228C=
ENST00000479320.5:n.1228C=
ENST00000495183.5:n.1230C=
ENST00000496081.5:n.804C=
NM_002116.7:c.987C=	NP_002107.3:p.Ala329=
NM_002116.8:c.987C= MANE Select	NP_002107.3:p.Ala329=