Canonical Allele Identifier: CA1619078749
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270008C= , CM000668.2:g.31270008C= GRCh38
NC_000006.11:g.31237785C= , CM000668.1:g.31237785C= GRCh37
NC_000006.10:g.31345764C= NCBI36
NG_029422.2:g.7124G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.973G= MANE Select ENSP00000365402.5:p.Gly325=
ENST00000376228.9:c.973G= ENSP00000365402.5:p.Gly325=
ENST00000376237.8:c.*560G= ENSP00000365412.4:n.*560G=
ENST00000383329.7:c.973G= ENSP00000372819.3:p.Gly325=
ENST00000470363.5:n.291G=
ENST00000487245.5:n.1332G=
NM_002117.5:c.973G= NP_002108.4:p.Gly325=
NM_002117.6:c.973G= MANE Select NP_002108.4:p.Gly325=