Canonical Allele Identifier: CA1619078745
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270007C= , CM000668.2:g.31270007C= GRCh38
NC_000006.11:g.31237784C= , CM000668.1:g.31237784C= GRCh37
NC_000006.10:g.31345763C= NCBI36
NG_029422.2:g.7125G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.974G= MANE Select ENSP00000365402.5:p.Gly325=
ENST00000376228.9:c.974G= ENSP00000365402.5:p.Gly325=
ENST00000376237.8:c.*561G= ENSP00000365412.4:n.*561G=
ENST00000383329.7:c.974G= ENSP00000372819.3:p.Gly325=
ENST00000470363.5:n.292G=
ENST00000487245.5:n.1333G=
NM_002117.5:c.974G= NP_002108.4:p.Gly325=
NM_002117.6:c.974G= MANE Select NP_002108.4:p.Gly325=