Canonical Allele Identifier: CA2677950673
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270354_31270355insA , CM000668.2:g.31270354_31270355insA GRCh38
NC_000006.11:g.31238131_31238132insA , CM000668.1:g.31238131_31238132insA GRCh37
NC_000006.10:g.31346110_31346111insA NCBI36
NG_029422.2:g.6777_6778insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.750_751insT MANE Select ENSP00000365402.5:p.Asp251Ter
ENST00000376228.9:c.750_751insT ENSP00000365402.5:p.Asp251Ter
ENST00000376237.8:c.*337_*338insT ENSP00000365412.4:n.*337_*338insT
ENST00000383329.7:c.750_751insT ENSP00000372819.3:p.Asp251Ter
ENST00000415537.1:c.665-24_665-23insT
ENST00000470363.5:n.68_69insT
ENST00000487245.5:n.1109_1110insT
ENST00000495835.1:n.939_940insT
NM_002117.5:c.750_751insT NP_002108.4:p.Asp251Ter
NM_002117.6:c.750_751insT MANE Select NP_002108.4:p.Asp251Ter