Canonical Allele Identifier: CA1619077169
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268930G= , CM000668.2:g.31268930G= GRCh38
NC_000006.11:g.31236707G= , CM000668.1:g.31236707G= GRCh37
NC_000006.10:g.31344686G= NCBI36
NG_029422.2:g.8202C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*239C= MANE Select ENSP00000365402.5:n.*239C=
ENST00000376228.9:c.*239C= ENSP00000365402.5:n.*239C=
ENST00000376237.8:c.*927C= ENSP00000365412.4:n.*927C=
ENST00000383329.7:c.*239C= ENSP00000372819.3:n.*239C=
ENST00000466892.5:n.573C=
ENST00000470363.5:n.1098C=
ENST00000487245.5:n.1699C=
NM_002117.5:c.*239C= NP_002108.4:n.*239C=
NM_002117.6:c.*239C= MANE Select NP_002108.4:n.*239C=