Canonical Allele Identifier: CA1619078025
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269515T= , CM000668.2:g.31269515T= GRCh38
NC_000006.11:g.31237292T= , CM000668.1:g.31237292T= GRCh37
NC_000006.10:g.31345271T= NCBI36
NG_029422.2:g.7617A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1026A= MANE Select ENSP00000365402.5:p.Gly342=
ENST00000376228.9:c.1026A= ENSP00000365402.5:p.Gly342=
ENST00000376237.8:c.*613A= ENSP00000365412.4:n.*613A=
ENST00000383329.7:c.1044A= ENSP00000372819.3:p.Gly348=
ENST00000466892.5:n.152A=
ENST00000470363.5:n.784A=
ENST00000487245.5:n.1385A=
NM_002117.5:c.1026A= NP_002108.4:p.Gly342=
NM_002117.6:c.1026A= MANE Select NP_002108.4:p.Gly342=