Canonical Allele Identifier: CA1619078055
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269534A= , CM000668.2:g.31269534A= GRCh38
NC_000006.11:g.31237311A= , CM000668.1:g.31237311A= GRCh37
NC_000006.10:g.31345290A= NCBI36
NG_029422.2:g.7598T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-9T= MANE Select ENSP00000365402.5:n.1016-9T=
ENST00000376228.9:c.1016-9T= ENSP00000365402.5:n.1016-9T=
ENST00000376237.8:c.*603-9T= ENSP00000365412.4:n.*603-9T=
ENST00000383329.7:c.1025T= ENSP00000372819.3:p.Leu342=
ENST00000466892.5:n.133T=
ENST00000470363.5:n.765T=
ENST00000487245.5:n.1375-9T=
NM_002117.5:c.1016-9T= NP_002108.4:n.1016-9T=
NM_002117.6:c.1016-9T= MANE Select NP_002108.4:n.1016-9T=