Canonical Allele Identifier: CA1087448908
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761090928

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268958_31268959del , CM000668.2:g.31268958_31268959del GRCh38
NC_000006.11:g.31236735_31236736del , CM000668.1:g.31236735_31236736del GRCh37
NC_000006.10:g.31344714_31344715del NCBI36
NG_029422.2:g.8173_8174del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*210_*211del MANE Select ENSP00000365402.5:n.*210_*211del
ENST00000376228.9:c.*210_*211del ENSP00000365402.5:n.*210_*211del
ENST00000376237.8:c.*898_*899del ENSP00000365412.4:n.*898_*899del
ENST00000383329.7:c.*210_*211del ENSP00000372819.3:n.*210_*211del
ENST00000466892.5:n.544_545del
ENST00000470363.5:n.1069_1070del
ENST00000487245.5:n.1670_1671del
NM_002117.5:c.*210_*211del NP_002108.4:n.*210_*211del
NM_002117.6:c.*210_*211del MANE Select NP_002108.4:n.*210_*211del