Canonical Allele Identifier: CA1619077342

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269122A= , CM000668.2:g.31269122A=	GRCh38
NC_000006.11:g.31236899A= , CM000668.1:g.31236899A=	GRCh37
NC_000006.10:g.31344878A=	NCBI36
NG_029422.2:g.8010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*47T= MANE Select	ENSP00000365402.5:n.*47T=
ENST00000376228.9:c.*47T=	ENSP00000365402.5:n.*47T=
ENST00000376237.8:c.*735T=	ENSP00000365412.4:n.*735T=
ENST00000383329.7:c.*47T=	ENSP00000372819.3:n.*47T=
ENST00000466892.5:n.381T=
ENST00000470363.5:n.906T=
ENST00000487245.5:n.1507T=
NM_002117.5:c.*47T=	NP_002108.4:n.*47T=
NM_002117.6:c.*47T= MANE Select	NP_002108.4:n.*47T=