Canonical Allele Identifier: CA917711584
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1554181751

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268943_31268944del , CM000668.2:g.31268943_31268944del GRCh38
NC_000006.11:g.31236720_31236721del , CM000668.1:g.31236720_31236721del GRCh37
NC_000006.10:g.31344699_31344700del NCBI36
NG_029422.2:g.8189_8190del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*226_*227del MANE Select ENSP00000365402.5:n.*226_*227del
ENST00000376228.9:c.*226_*227del ENSP00000365402.5:n.*226_*227del
ENST00000376237.8:c.*914_*915del ENSP00000365412.4:n.*914_*915del
ENST00000383329.7:c.*226_*227del ENSP00000372819.3:n.*226_*227del
ENST00000466892.5:n.560_561del
ENST00000470363.5:n.1085_1086del
ENST00000487245.5:n.1686_1687del
NM_002117.5:c.*226_*227del NP_002108.4:n.*226_*227del
NM_002117.6:c.*226_*227del MANE Select NP_002108.4:n.*226_*227del