Canonical Allele Identifier: CA1619078619

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269981T= , CM000668.2:g.31269981T=	GRCh38
NC_000006.11:g.31237758T= , CM000668.1:g.31237758T=	GRCh37
NC_000006.10:g.31345737T=	NCBI36
NG_029422.2:g.7151A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.1000A= MANE Select	ENSP00000365402.5:p.Arg334=
ENST00000376228.9:c.1000A=	ENSP00000365402.5:p.Arg334=
ENST00000376237.8:c.*587A=	ENSP00000365412.4:n.*587A=
ENST00000383329.7:c.1000A=	ENSP00000372819.3:p.Arg334=
ENST00000470363.5:n.318A=
ENST00000487245.5:n.1359A=
NM_002117.5:c.1000A=	NP_002108.4:p.Arg334=
NM_002117.6:c.1000A= MANE Select	NP_002108.4:p.Arg334=