Canonical Allele Identifier: CA3710384
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs776231802

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270049_31270050insCAGC , CM000668.2:g.31270049_31270050insCAGC GRCh38
NC_000006.11:g.31237826_31237827insCAGC , CM000668.1:g.31237826_31237827insCAGC GRCh37
NC_000006.10:g.31345805_31345806insCAGC NCBI36
NG_029422.2:g.7082_7083insGCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.931_932insGCTG MANE Select ENSP00000365402.5:p.Ile311SerfsTer25
ENST00000376228.9:c.931_932insGCTG ENSP00000365402.5:p.Ile311SerfsTer25
ENST00000376237.8:c.*518_*519insGCTG ENSP00000365412.4:n.*518_*519insGCTG
ENST00000383329.7:c.931_932insGCTG ENSP00000372819.3:p.Ile311SerfsTer25
ENST00000470363.5:n.249_250insGCTG
ENST00000487245.5:n.1290_1291insGCTG
NM_002117.5:c.931_932insGCTG NP_002108.4:p.Ile311SerfsTer25
NM_002117.6:c.931_932insGCTG MANE Select NP_002108.4:p.Ile311SerfsTer25