Canonical Allele Identifier: CA2677951353
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271331_31271332insGCCA , CM000668.2:g.31271331_31271332insGCCA GRCh38
NC_000006.11:g.31239108_31239109insGCCA , CM000668.1:g.31239108_31239109insGCCA GRCh37
NC_000006.10:g.31347087_31347088insGCCA NCBI36
NG_029422.2:g.5800_5801insTGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.360_361insTGGC MANE Select ENSP00000365402.5:p.Arg121TrpfsTer19
ENST00000376228.9:c.360_361insTGGC ENSP00000365402.5:p.Arg121TrpfsTer19
ENST00000376237.8:c.344-1_344insTGGC ENSP00000365412.4:n.344-1_344insTGGC
ENST00000383329.7:c.360_361insTGGC ENSP00000372819.3:p.Arg121TrpfsTer19
ENST00000415537.1:c.358_359insTGGC
ENST00000484378.1:n.629_630insTGGC
ENST00000487245.5:n.719_720insTGGC
ENST00000495835.1:n.549_550insTGGC
NM_002117.5:c.360_361insTGGC NP_002108.4:p.Arg121TrpfsTer19
NM_002117.6:c.360_361insTGGC MANE Select NP_002108.4:p.Arg121TrpfsTer19