Canonical Allele Identifier: CA2677951259
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271142_31271154del , CM000668.2:g.31271142_31271154del GRCh38
NC_000006.11:g.31238919_31238931del , CM000668.1:g.31238919_31238931del GRCh37
NC_000006.10:g.31346898_31346910del NCBI36
NG_029422.2:g.5978_5990del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.538_550del MANE Select ENSP00000365402.5:p.Leu180TrpfsTer30
ENST00000376228.9:c.538_550del ENSP00000365402.5:p.Leu180TrpfsTer30
ENST00000376237.8:c.*125_*137del ENSP00000365412.4:n.*125_*137del
ENST00000383329.7:c.538_550del ENSP00000372819.3:p.Leu180TrpfsTer30
ENST00000415537.1:c.536_548del
ENST00000484378.1:n.807_819del
ENST00000487245.5:n.897_909del
ENST00000495835.1:n.727_739del
NM_002117.5:c.538_550del NP_002108.4:p.Leu180TrpfsTer30
NM_002117.6:c.538_550del MANE Select NP_002108.4:p.Leu180TrpfsTer30