Canonical Allele Identifier: CA2677951312
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271230del , CM000668.2:g.31271230del GRCh38
NC_000006.11:g.31239007del , CM000668.1:g.31239007del GRCh37
NC_000006.10:g.31346986del NCBI36
NG_029422.2:g.5902del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.462del MANE Select ENSP00000365402.5:p.Arg155AlafsTer26
ENST00000376228.9:c.462del ENSP00000365402.5:p.Arg155AlafsTer26
ENST00000376237.8:c.*49del ENSP00000365412.4:n.*49del
ENST00000383329.7:c.462del ENSP00000372819.3:p.Arg155AlafsTer26
ENST00000415537.1:c.460del
ENST00000484378.1:n.731del
ENST00000487245.5:n.821del
ENST00000495835.1:n.651del
NM_002117.5:c.462del NP_002108.4:p.Arg155AlafsTer26
NM_002117.6:c.462del MANE Select NP_002108.4:p.Arg155AlafsTer26