Canonical Allele Identifier: CA1619080372
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271162G= , CM000668.2:g.31271162G= GRCh38
NC_000006.11:g.31238939G= , CM000668.1:g.31238939G= GRCh37
NC_000006.10:g.31346918G= NCBI36
NG_029422.2:g.5970C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.530C= MANE Select ENSP00000365402.5:p.Ala177=
ENST00000376228.9:c.530C= ENSP00000365402.5:p.Ala177=
ENST00000376237.8:c.*117C= ENSP00000365412.4:n.*117C=
ENST00000383329.7:c.530C= ENSP00000372819.3:p.Ala177=
ENST00000415537.1:c.528C=
ENST00000484378.1:n.799C=
ENST00000487245.5:n.889C=
ENST00000495835.1:n.719C=
NM_002117.5:c.530C= NP_002108.4:p.Ala177=
NM_002117.6:c.530C= MANE Select NP_002108.4:p.Ala177=