Canonical Allele Identifier: CA1619078392

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269781A= , CM000668.2:g.31269781A=	GRCh38
NC_000006.11:g.31237558A= , CM000668.1:g.31237558A=	GRCh37
NC_000006.10:g.31345537A=	NCBI36
NG_029422.2:g.7351T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+185T= MANE Select	ENSP00000365402.5:n.1015+185T=
ENST00000376228.9:c.1015+185T=	ENSP00000365402.5:n.1015+185T=
ENST00000376237.8:c.*602+185T=	ENSP00000365412.4:n.*602+185T=
ENST00000383329.7:c.1015+185T=	ENSP00000372819.3:n.1015+185T=
ENST00000470363.5:n.518T=
ENST00000487245.5:n.1374+185T=
NM_002117.5:c.1015+185T=	NP_002108.4:n.1015+185T=
NM_002117.6:c.1015+185T= MANE Select	NP_002108.4:n.1015+185T=