Canonical Allele Identifier: CA1619077228

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269020G= , CM000668.2:g.31269020G=	GRCh38
NC_000006.11:g.31236797G= , CM000668.1:g.31236797G=	GRCh37
NC_000006.10:g.31344776G=	NCBI36
NG_029422.2:g.8112C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*149C= MANE Select	ENSP00000365402.5:n.*149C=
ENST00000376228.9:c.*149C=	ENSP00000365402.5:n.*149C=
ENST00000376237.8:c.*837C=	ENSP00000365412.4:n.*837C=
ENST00000383329.7:c.*149C=	ENSP00000372819.3:n.*149C=
ENST00000466892.5:n.483C=
ENST00000470363.5:n.1008C=
ENST00000487245.5:n.1609C=
NM_002117.5:c.*149C=	NP_002108.4:n.*149C=
NM_002117.6:c.*149C= MANE Select	NP_002108.4:n.*149C=