Canonical Allele Identifier: CA2677951306
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271212del , CM000668.2:g.31271212del GRCh38
NC_000006.11:g.31238989del , CM000668.1:g.31238989del GRCh37
NC_000006.10:g.31346968del NCBI36
NG_029422.2:g.5921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.481del MANE Select ENSP00000365402.5:p.Asp161ThrfsTer20
ENST00000376228.9:c.481del ENSP00000365402.5:p.Asp161ThrfsTer20
ENST00000376237.8:c.*68del ENSP00000365412.4:n.*68del
ENST00000383329.7:c.481del ENSP00000372819.3:p.Asp161ThrfsTer20
ENST00000415537.1:c.479del
ENST00000484378.1:n.750del
ENST00000487245.5:n.840del
ENST00000495835.1:n.670del
NM_002117.5:c.481del NP_002108.4:p.Asp161ThrfsTer20
NM_002117.6:c.481del MANE Select NP_002108.4:p.Asp161ThrfsTer20