Canonical Allele Identifier: CA2677949620
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269314del , CM000668.2:g.31269314del GRCh38
NC_000006.11:g.31237091del , CM000668.1:g.31237091del GRCh37
NC_000006.10:g.31345070del NCBI36
NG_029422.2:g.7819del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+25del MANE Select ENSP00000365402.5:n.1096+25del
ENST00000376228.9:c.1096+25del ENSP00000365402.5:n.1096+25del
ENST00000376237.8:c.*683+25del ENSP00000365412.4:n.*683+25del
ENST00000383329.7:c.1114+25del ENSP00000372819.3:n.1114+25del
ENST00000466892.5:n.329+25del
ENST00000470363.5:n.854+25del
ENST00000487245.5:n.1455+25del
NM_002117.5:c.1096+25del NP_002108.4:n.1096+25del
NM_002117.6:c.1096+25del MANE Select NP_002108.4:n.1096+25del