Canonical Allele Identifier: CA1619077787
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269395A= , CM000668.2:g.31269395A= GRCh38
NC_000006.11:g.31237172A= , CM000668.1:g.31237172A= GRCh37
NC_000006.10:g.31345151A= NCBI36
NG_029422.2:g.7737T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1049-10T= MANE Select ENSP00000365402.5:n.1049-10T=
ENST00000376228.9:c.1049-10T= ENSP00000365402.5:n.1049-10T=
ENST00000376237.8:c.*636-10T= ENSP00000365412.4:n.*636-10T=
ENST00000383329.7:c.1067-10T= ENSP00000372819.3:n.1067-10T=
ENST00000466892.5:n.272T=
ENST00000470363.5:n.807-10T=
ENST00000487245.5:n.1408-10T=
NM_002117.5:c.1049-10T= NP_002108.4:n.1049-10T=
NM_002117.6:c.1049-10T= MANE Select NP_002108.4:n.1049-10T=