Canonical Allele Identifier: CA1619080525
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271329C= , CM000668.2:g.31271329C= GRCh38
NC_000006.11:g.31239106C= , CM000668.1:g.31239106C= GRCh37
NC_000006.10:g.31347085C= NCBI36
NG_029422.2:g.5803G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.363G= MANE Select ENSP00000365402.5:p.Arg121=
ENST00000376228.9:c.363G= ENSP00000365402.5:p.Arg121=
ENST00000376237.8:c.346G= ENSP00000365412.4:p.Asp116=
ENST00000383329.7:c.363G= ENSP00000372819.3:p.Arg121=
ENST00000415537.1:c.361G=
ENST00000484378.1:n.632G=
ENST00000487245.5:n.722G=
ENST00000495835.1:n.552G=
NM_002117.5:c.363G= NP_002108.4:p.Arg121=
NM_002117.6:c.363G= MANE Select NP_002108.4:p.Arg121=