Canonical Allele Identifier: CA917710715
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9279071

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271494_31271495del , CM000668.2:g.31271494_31271495del GRCh38
NC_000006.11:g.31239271_31239272del , CM000668.1:g.31239271_31239272del GRCh37
NC_000006.10:g.31347250_31347251del NCBI36
NG_029422.2:g.5637_5638del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+104_343+105del MANE Select ENSP00000365402.5:n.343+104_343+105del
ENST00000376228.9:c.343+104_343+105del ENSP00000365402.5:n.343+104_343+105del
ENST00000376237.8:c.343+104_343+105del ENSP00000365412.4:n.343+104_343+105del
ENST00000383329.7:c.343+104_343+105del ENSP00000372819.3:n.343+104_343+105del
ENST00000415537.1:c.341+104_341+105del
ENST00000484378.1:n.466_467del
ENST00000487245.5:n.556_557del
ENST00000495835.1:n.532+104_532+105del
NM_002117.5:c.343+104_343+105del NP_002108.4:n.343+104_343+105del
NM_002117.6:c.343+104_343+105del MANE Select NP_002108.4:n.343+104_343+105del