Canonical Allele Identifier: CA1619080370
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271160C= , CM000668.2:g.31271160C= GRCh38
NC_000006.11:g.31238937C= , CM000668.1:g.31238937C= GRCh37
NC_000006.10:g.31346916C= NCBI36
NG_029422.2:g.5972G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.532G= MANE Select ENSP00000365402.5:p.Glu178=
ENST00000376228.9:c.532G= ENSP00000365402.5:p.Glu178=
ENST00000376237.8:c.*119G= ENSP00000365412.4:n.*119G=
ENST00000383329.7:c.532G= ENSP00000372819.3:p.Glu178=
ENST00000415537.1:c.530G=
ENST00000484378.1:n.801G=
ENST00000487245.5:n.891G=
ENST00000495835.1:n.721G=
NM_002117.5:c.532G= NP_002108.4:p.Glu178=
NM_002117.6:c.532G= MANE Select NP_002108.4:p.Glu178=