Canonical Allele Identifier: CA3710364
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs780546377

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270008_31270009insT , CM000668.2:g.31270008_31270009insT GRCh38
NC_000006.11:g.31237785_31237786insT , CM000668.1:g.31237785_31237786insT GRCh37
NC_000006.10:g.31345764_31345765insT NCBI36
NG_029422.2:g.7123_7124insA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.972_973insA MANE Select ENSP00000365402.5:p.Gly325ArgfsTer10
ENST00000376228.9:c.972_973insA ENSP00000365402.5:p.Gly325ArgfsTer10
ENST00000376237.8:c.*559_*560insA ENSP00000365412.4:n.*559_*560insA
ENST00000383329.7:c.972_973insA ENSP00000372819.3:p.Gly325ArgfsTer10
ENST00000470363.5:n.290_291insA
ENST00000487245.5:n.1331_1332insA
NM_002117.5:c.972_973insA NP_002108.4:p.Gly325ArgfsTer10
NM_002117.6:c.972_973insA MANE Select NP_002108.4:p.Gly325ArgfsTer10