Canonical Allele Identifier: CA136866466
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860533

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271122del , CM000668.2:g.31271122del GRCh38
NC_000006.11:g.31238899del , CM000668.1:g.31238899del GRCh37
NC_000006.10:g.31346878del NCBI36
NG_029422.2:g.6010del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.570del MANE Select ENSP00000365402.5:p.Glu190AspfsTer24
ENST00000376228.9:c.570del ENSP00000365402.5:p.Glu190AspfsTer24
ENST00000376237.8:c.*157del ENSP00000365412.4:n.*157del
ENST00000383329.7:c.570del ENSP00000372819.3:p.Glu190AspfsTer24
ENST00000415537.1:c.568del
ENST00000484378.1:n.839del
ENST00000487245.5:n.929del
ENST00000495835.1:n.759del
NM_002117.5:c.570del NP_002108.4:p.Glu190AspfsTer24
NM_002117.6:c.570del MANE Select NP_002108.4:p.Glu190AspfsTer24