Canonical Allele Identifier: CA2677951310
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271223del , CM000668.2:g.31271223del GRCh38
NC_000006.11:g.31239000del , CM000668.1:g.31239000del GRCh37
NC_000006.10:g.31346979del NCBI36
NG_029422.2:g.5909del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.469del MANE Select ENSP00000365402.5:p.Trp157GlyfsTer24
ENST00000376228.9:c.469del ENSP00000365402.5:p.Trp157GlyfsTer24
ENST00000376237.8:c.*56del ENSP00000365412.4:n.*56del
ENST00000383329.7:c.469del ENSP00000372819.3:p.Trp157GlyfsTer24
ENST00000415537.1:c.467del
ENST00000484378.1:n.738del
ENST00000487245.5:n.828del
ENST00000495835.1:n.658del
NM_002117.5:c.469del NP_002108.4:p.Trp157GlyfsTer24
NM_002117.6:c.469del MANE Select NP_002108.4:p.Trp157GlyfsTer24