Canonical Allele Identifier: CA2677951264
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271147del , CM000668.2:g.31271147del GRCh38
NC_000006.11:g.31238924del , CM000668.1:g.31238924del GRCh37
NC_000006.10:g.31346903del NCBI36
NG_029422.2:g.5986del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.546del MANE Select ENSP00000365402.5:p.Tyr183ThrfsTer?
ENST00000376228.9:c.546del ENSP00000365402.5:p.Tyr183ThrfsTer?
ENST00000376237.8:c.*133del ENSP00000365412.4:n.*133del
ENST00000383329.7:c.546del ENSP00000372819.3:p.Tyr183ThrfsTer?
ENST00000415537.1:c.544del
ENST00000484378.1:n.815del
ENST00000487245.5:n.905del
ENST00000495835.1:n.735del
NM_002117.5:c.546del NP_002108.4:p.Tyr183ThrfsTer?
NM_002117.6:c.546del MANE Select NP_002108.4:p.Tyr183ThrfsTer?