Canonical Allele Identifier: CA566688986
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270228del , CM000668.2:g.31270228del GRCh38
NC_000006.11:g.31238005del , CM000668.1:g.31238005del GRCh37
NC_000006.10:g.31345984del NCBI36
NG_029422.2:g.6907del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.880del MANE Select ENSP00000365402.5:p.Leu294SerfsTer3
ENST00000376228.9:c.880del ENSP00000365402.5:p.Leu294SerfsTer3
ENST00000376237.8:c.*467del ENSP00000365412.4:n.*467del
ENST00000383329.7:c.880del ENSP00000372819.3:p.Leu294SerfsTer3
ENST00000415537.1:c.771del
ENST00000470363.5:n.198del
ENST00000487245.5:n.1239del
ENST00000495835.1:n.1069del
NM_002117.5:c.880del NP_002108.4:p.Leu294SerfsTer3
NM_002117.6:c.880del MANE Select NP_002108.4:p.Leu294SerfsTer3