Canonical Allele Identifier: CA3710366
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs749599742

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270009_31270010insGGACAGCT , CM000668.2:g.31270009_31270010insGGACAGCT GRCh38
NC_000006.11:g.31237786_31237787insGGACAGCT , CM000668.1:g.31237786_31237787insGGACAGCT GRCh37
NC_000006.10:g.31345765_31345766insGGACAGCT NCBI36
NG_029422.2:g.7122_7123insAGCTGTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.971_972insAGCTGTCC MANE Select ENSP00000365402.5:p.Gly325AlafsTer10
ENST00000376228.9:c.971_972insAGCTGTCC ENSP00000365402.5:p.Gly325AlafsTer10
ENST00000376237.8:c.*558_*559insAGCTGTCC ENSP00000365412.4:n.*558_*559insAGCTGTCC
ENST00000383329.7:c.971_972insAGCTGTCC ENSP00000372819.3:p.Gly325AlafsTer10
ENST00000470363.5:n.289_290insAGCTGTCC
ENST00000487245.5:n.1330_1331insAGCTGTCC
NM_002117.5:c.971_972insAGCTGTCC NP_002108.4:p.Gly325AlafsTer10
NM_002117.6:c.971_972insAGCTGTCC MANE Select NP_002108.4:p.Gly325AlafsTer10