Canonical Allele Identifier: CA2677949657
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269373dup , CM000668.2:g.31269373dup GRCh38
NC_000006.11:g.31237150dup , CM000668.1:g.31237150dup GRCh37
NC_000006.10:g.31345129dup NCBI36
NG_029422.2:g.7761dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1063dup MANE Select ENSP00000365402.5:p.Gln355ProfsTer4
ENST00000376228.9:c.1063dup ENSP00000365402.5:p.Gln355ProfsTer4
ENST00000376237.8:c.*650dup ENSP00000365412.4:n.*650dup
ENST00000383329.7:c.1081dup ENSP00000372819.3:p.Gln361ProfsTer4
ENST00000466892.5:n.296dup
ENST00000470363.5:n.821dup
ENST00000487245.5:n.1422dup
NM_002117.5:c.1063dup NP_002108.4:p.Gln355ProfsTer4
NM_002117.6:c.1063dup MANE Select NP_002108.4:p.Gln355ProfsTer4