Canonical Allele Identifier: CA2677951299
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271199_31271201del , CM000668.2:g.31271199_31271201del GRCh38
NC_000006.11:g.31238976_31238978del , CM000668.1:g.31238976_31238978del GRCh37
NC_000006.10:g.31346955_31346957del NCBI36
NG_029422.2:g.5931_5933del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.491_493del MANE Select ENSP00000365402.5:p.Ala164_Gln165delinsGlu
ENST00000376228.9:c.491_493del ENSP00000365402.5:p.Ala164_Gln165delinsGlu
ENST00000376237.8:c.*78_*80del ENSP00000365412.4:n.*78_*80del
ENST00000383329.7:c.491_493del ENSP00000372819.3:p.Ala164_Gln165delinsGlu
ENST00000415537.1:c.489_491del
ENST00000484378.1:n.760_762del
ENST00000487245.5:n.850_852del
ENST00000495835.1:n.680_682del
NM_002117.5:c.491_493del NP_002108.4:p.Ala164_Gln165delinsGlu
NM_002117.6:c.491_493del MANE Select NP_002108.4:p.Ala164_Gln165delinsGlu