Canonical Allele Identifier: CA432423454
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149851del , CM000665.2:g.10149851del GRCh38
NC_000003.11:g.10191535del , CM000665.1:g.10191535del GRCh37
NC_000003.10:g.10166535del NCBI36
NG_008212.3:g.13217del , LRG_322:g.13217del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*205del ENSP00000512434.1:n.*205del
ENST00000696143.1:c.664del ENSP00000512435.1:n.664del
ENST00000696153.1:c.639del ENSP00000512444.1:p.Arg214AspfsTer25
ENST00000256474.3:c.528del MANE Select ENSP00000256474.3:p.Arg177AspfsTer25
ENST00000256474.2:c.528del ENSP00000256474.2:p.Arg177AspfsTer25
ENST00000345392.2:c.405del ENSP00000344757.2:p.Arg136AspfsTer25
ENST00000477538.1:n.664del
NM_000551.3:c.528del , LRG_322t1:c.528del NP_000542.1:p.Arg177AspfsTer25
NM_198156.2:c.405del NP_937799.1:p.Arg136AspfsTer25
NM_001354723.1:c.*82del NP_001341652.1:n.*82del
NM_000551.4:c.528del MANE Select NP_000542.1:p.Arg177AspfsTer25
NM_001354723.2:c.*82del NP_001341652.1:n.*82del
NM_198156.3:c.405del NP_937799.1:p.Arg136AspfsTer25