Canonical Allele Identifier: CA2677950293
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269991_31269992insACAG , CM000668.2:g.31269991_31269992insACAG GRCh38
NC_000006.11:g.31237768_31237769insACAG , CM000668.1:g.31237768_31237769insACAG GRCh37
NC_000006.10:g.31345747_31345748insACAG NCBI36
NG_029422.2:g.7140_7141insCTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.989_990insCTGT MANE Select ENSP00000365402.5:p.Met331CysfsTer5
ENST00000376228.9:c.989_990insCTGT ENSP00000365402.5:p.Met331CysfsTer5
ENST00000376237.8:c.*576_*577insCTGT ENSP00000365412.4:n.*576_*577insCTGT
ENST00000383329.7:c.989_990insCTGT ENSP00000372819.3:p.Met331CysfsTer5
ENST00000470363.5:n.307_308insCTGT
ENST00000487245.5:n.1348_1349insCTGT
NM_002117.5:c.989_990insCTGT NP_002108.4:p.Met331CysfsTer5
NM_002117.6:c.989_990insCTGT MANE Select NP_002108.4:p.Met331CysfsTer5