Canonical Allele Identifier: CA1619080378

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271169G= , CM000668.2:g.31271169G=	GRCh38
NC_000006.11:g.31238946G= , CM000668.1:g.31238946G=	GRCh37
NC_000006.10:g.31346925G=	NCBI36
NG_029422.2:g.5963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.523C= MANE Select	ENSP00000365402.5:p.Arg175=
ENST00000376228.9:c.523C=	ENSP00000365402.5:p.Arg175=
ENST00000376237.8:c.*110C=	ENSP00000365412.4:n.*110C=
ENST00000383329.7:c.523C=	ENSP00000372819.3:p.Arg175=
ENST00000415537.1:c.521C=
ENST00000484378.1:n.792C=
ENST00000487245.5:n.882C=
ENST00000495835.1:n.712C=
NM_002117.5:c.523C=	NP_002108.4:p.Arg175=
NM_002117.6:c.523C= MANE Select	NP_002108.4:p.Arg175=