Canonical Allele Identifier: CA432423671
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM14337
MyVariant Identifiers: chr3:g.10191569del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149885del , CM000665.2:g.10149885del GRCh38
NC_000003.11:g.10191569del , CM000665.1:g.10191569del GRCh37
NC_000003.10:g.10166569del NCBI36
NG_008212.3:g.13251del , LRG_322:g.13251del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*239del ENSP00000512434.1:n.*239del
ENST00000696143.1:c.698del ENSP00000512435.1:n.698del
ENST00000696153.1:c.673del ENSP00000512444.1:p.Leu225TrpfsTer14
ENST00000256474.3:c.562del MANE Select ENSP00000256474.3:p.Leu188TrpfsTer14
ENST00000256474.2:c.562del ENSP00000256474.2:p.Leu188TrpfsTer14
ENST00000345392.2:c.439del ENSP00000344757.2:p.Leu147TrpfsTer14
ENST00000477538.1:n.698del
NM_000551.3:c.562del , LRG_322t1:c.562del NP_000542.1:p.Leu188TrpfsTer14
NM_198156.2:c.439del NP_937799.1:p.Leu147TrpfsTer14
NM_001354723.1:c.*116del NP_001341652.1:n.*116del
NM_000551.4:c.562del MANE Select NP_000542.1:p.Leu188TrpfsTer14
NM_001354723.2:c.*116del NP_001341652.1:n.*116del
NM_198156.3:c.439del NP_937799.1:p.Leu147TrpfsTer14