Canonical Allele Identifier: CA1619077110

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268820A= , CM000668.2:g.31268820A=	GRCh38
NC_000006.11:g.31236597A= , CM000668.1:g.31236597A=	GRCh37
NC_000006.10:g.31344576A=	NCBI36
NG_029422.2:g.8312T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.*349T= MANE Select	ENSP00000365402.5:n.*349T=
ENST00000376228.9:c.*349T=	ENSP00000365402.5:n.*349T=
ENST00000376237.8:c.*1037T=	ENSP00000365412.4:n.*1037T=
ENST00000383329.7:c.*349T=	ENSP00000372819.3:n.*349T=
ENST00000466892.5:n.683T=
ENST00000470363.5:n.1208T=
ENST00000487245.5:n.1809T=
NM_002117.5:c.*349T=	NP_002108.4:n.*349T=
NM_002117.6:c.*349T= MANE Select	NP_002108.4:n.*349T=