Canonical Allele Identifier: CA1619080543

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271342T= , CM000668.2:g.31271342T=	GRCh38
NC_000006.11:g.31239119T= , CM000668.1:g.31239119T=	GRCh37
NC_000006.10:g.31347098T=	NCBI36
NG_029422.2:g.5790A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.350A= MANE Select	ENSP00000365402.5:p.His117=
ENST00000376228.9:c.350A=	ENSP00000365402.5:p.His117=
ENST00000376237.8:c.344-11A=	ENSP00000365412.4:n.344-11A=
ENST00000383329.7:c.350A=	ENSP00000372819.3:p.His117=
ENST00000415537.1:c.348A=
ENST00000484378.1:n.619A=
ENST00000487245.5:n.709A=
ENST00000495835.1:n.539A=
NM_002117.5:c.350A=	NP_002108.4:p.His117=
NM_002117.6:c.350A= MANE Select	NP_002108.4:p.His117=