Canonical Allele Identifier: CA2844096477
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271298_31271299insT , CM000668.2:g.31271298_31271299insT GRCh38
NC_000006.11:g.31239075_31239076insT , CM000668.1:g.31239075_31239076insT GRCh37
NC_000006.10:g.31347054_31347055insT NCBI36
NG_029422.2:g.5833_5834insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.393_394insA MANE Select ENSP00000365402.5:p.Arg132ThrfsTer7
ENST00000376228.9:c.393_394insA ENSP00000365402.5:p.Arg132ThrfsTer7
ENST00000376237.8:c.376_377insA ENSP00000365412.4:p.Ala126AspfsTer20
ENST00000383329.7:c.393_394insA ENSP00000372819.3:p.Arg132ThrfsTer7
ENST00000415537.1:c.391_392insA
ENST00000484378.1:n.662_663insA
ENST00000487245.5:n.752_753insA
ENST00000495835.1:n.582_583insA
NM_002117.5:c.393_394insA NP_002108.4:p.Arg132ThrfsTer7
NM_002117.6:c.393_394insA MANE Select NP_002108.4:p.Arg132ThrfsTer7