Canonical Allele Identifier: CA2677950278
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269982_31269984del , CM000668.2:g.31269982_31269984del GRCh38
NC_000006.11:g.31237759_31237761del , CM000668.1:g.31237759_31237761del GRCh37
NC_000006.10:g.31345738_31345740del NCBI36
NG_029422.2:g.7148_7150del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.997_999del MANE Select ENSP00000365402.5:p.Cys333del
ENST00000376228.9:c.997_999del ENSP00000365402.5:p.Cys333del
ENST00000376237.8:c.*584_*586del ENSP00000365412.4:n.*584_*586del
ENST00000383329.7:c.997_999del ENSP00000372819.3:p.Cys333del
ENST00000470363.5:n.315_317del
ENST00000487245.5:n.1356_1358del
NM_002117.5:c.997_999del NP_002108.4:p.Cys333del
NM_002117.6:c.997_999del MANE Select NP_002108.4:p.Cys333del