Canonical Allele Identifier: CA1619080421
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271213G= , CM000668.2:g.31271213G= GRCh38
NC_000006.11:g.31238990G= , CM000668.1:g.31238990G= GRCh37
NC_000006.10:g.31346969G= NCBI36
NG_029422.2:g.5919C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.479C= MANE Select ENSP00000365402.5:p.Ala160=
ENST00000376228.9:c.479C= ENSP00000365402.5:p.Ala160=
ENST00000376237.8:c.*66C= ENSP00000365412.4:n.*66C=
ENST00000383329.7:c.479C= ENSP00000372819.3:p.Ala160=
ENST00000415537.1:c.477C=
ENST00000484378.1:n.748C=
ENST00000487245.5:n.838C=
ENST00000495835.1:n.668C=
NM_002117.5:c.479C= NP_002108.4:p.Ala160=
NM_002117.6:c.479C= MANE Select NP_002108.4:p.Ala160=