Canonical Allele Identifier: CA351753724
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1732864
ClinVar RCV Id: RCV002455064
dbSNP Id: rs1559428077
COSMIC: COSM97146

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146530C>A , CM000665.2:g.10146530C>A GRCh38
NC_000003.11:g.10188214C>A , CM000665.1:g.10188214C>A GRCh37
NC_000003.10:g.10163214C>A NCBI36
NG_008212.3:g.9896C>A , LRG_322:g.9896C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*34C>A ENSP00000512434.1:n.*34C>A
ENST00000696143.1:c.600-3257C>A ENSP00000512435.1:n.600-3257C>A
ENST00000696153.1:c.357C>A ENSP00000512444.1:p.Phe119Leu
ENST00000256474.3:c.357C>A MANE Select ENSP00000256474.3:p.Phe119Leu
ENST00000256474.2:c.357C>A ENSP00000256474.2:p.Phe119Leu
ENST00000345392.2:c.341-3257C>A ENSP00000344757.2:n.341-3257C>A
ENST00000477538.1:n.493C>A
NM_000551.3:c.357C>A , LRG_322t1:c.357C>A NP_000542.1:p.Phe119Leu
NM_198156.2:c.341-3257C>A NP_937799.1:n.341-3257C>A
XM_011534078.1:c.*34C>A XP_011532380.1:n.*34C>A
NM_001354723.1:c.*18-3257C>A NP_001341652.1:n.*18-3257C>A
NM_000551.4:c.357C>A MANE Select NP_000542.1:p.Phe119Leu
NM_001354723.2:c.*18-3257C>A NP_001341652.1:n.*18-3257C>A
NM_198156.3:c.341-3257C>A NP_937799.1:n.341-3257C>A