Canonical Allele Identifier: CA040622
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 386138
dbSNP Id: rs372340900
gnomAD v2: 3-10188193-G-A
gnomAD v3: 3-10146509-G-A
gnomAD v4: 3-10146509-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146509G>A , CM000665.2:g.10146509G>A GRCh38
NC_000003.11:g.10188193G>A , CM000665.1:g.10188193G>A GRCh37
NC_000003.10:g.10163193G>A NCBI36
NG_008212.3:g.9875G>A , LRG_322:g.9875G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*18-5G>A ENSP00000512434.1:n.*18-5G>A
ENST00000696143.1:c.600-3278G>A ENSP00000512435.1:n.600-3278G>A
ENST00000696153.1:c.341-5G>A ENSP00000512444.1:n.341-5G>A
ENST00000256474.3:c.341-5G>A MANE Select ENSP00000256474.3:n.341-5G>A
ENST00000256474.2:c.341-5G>A ENSP00000256474.2:n.341-5G>A
ENST00000345392.2:c.341-3278G>A ENSP00000344757.2:n.341-3278G>A
ENST00000477538.1:n.477-5G>A
NM_000551.3:c.341-5G>A , LRG_322t1:c.341-5G>A NP_000542.1:n.341-5G>A
NM_198156.2:c.341-3278G>A NP_937799.1:n.341-3278G>A
XM_011534078.1:c.*18-5G>A XP_011532380.1:n.*18-5G>A
NM_001354723.1:c.*18-3278G>A NP_001341652.1:n.*18-3278G>A
NM_000551.4:c.341-5G>A MANE Select NP_000542.1:n.341-5G>A
NM_001354723.2:c.*18-3278G>A NP_001341652.1:n.*18-3278G>A
NM_198156.3:c.341-3278G>A NP_937799.1:n.341-3278G>A