Canonical Allele Identifier: CA351754021
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs2125128369
COSMIC: COSM33993

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146577T>A , CM000665.2:g.10146577T>A GRCh38
NC_000003.11:g.10188261T>A , CM000665.1:g.10188261T>A GRCh37
NC_000003.10:g.10163261T>A NCBI36
NG_008212.3:g.9943T>A , LRG_322:g.9943T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*81T>A ENSP00000512434.1:n.*81T>A
ENST00000696143.1:c.600-3210T>A ENSP00000512435.1:n.600-3210T>A
ENST00000696153.1:c.404T>A ENSP00000512444.1:p.Leu135Ter
ENST00000256474.3:c.404T>A MANE Select ENSP00000256474.3:p.Leu135Ter
ENST00000256474.2:c.404T>A ENSP00000256474.2:p.Leu135Ter
ENST00000345392.2:c.341-3210T>A ENSP00000344757.2:n.341-3210T>A
ENST00000477538.1:n.540T>A
NM_000551.3:c.404T>A , LRG_322t1:c.404T>A NP_000542.1:p.Leu135Ter
NM_198156.2:c.341-3210T>A NP_937799.1:n.341-3210T>A
XM_011534078.1:c.*81T>A XP_011532380.1:n.*81T>A
NM_001354723.1:c.*18-3210T>A NP_001341652.1:n.*18-3210T>A
NM_000551.4:c.404T>A MANE Select NP_000542.1:p.Leu135Ter
NM_001354723.2:c.*18-3210T>A NP_001341652.1:n.*18-3210T>A
NM_198156.3:c.341-3210T>A NP_937799.1:n.341-3210T>A