Canonical Allele Identifier: CA1619080516
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271319A= , CM000668.2:g.31271319A= GRCh38
NC_000006.11:g.31239096A= , CM000668.1:g.31239096A= GRCh37
NC_000006.10:g.31347075A= NCBI36
NG_029422.2:g.5813T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.373T= MANE Select ENSP00000365402.5:p.Cys125=
ENST00000376228.9:c.373T= ENSP00000365402.5:p.Cys125=
ENST00000376237.8:c.356T= ENSP00000365412.4:p.Leu119=
ENST00000383329.7:c.373T= ENSP00000372819.3:p.Cys125=
ENST00000415537.1:c.371T=
ENST00000484378.1:n.642T=
ENST00000487245.5:n.732T=
ENST00000495835.1:n.562T=
NM_002117.5:c.373T= NP_002108.4:p.Cys125=
NM_002117.6:c.373T= MANE Select NP_002108.4:p.Cys125=