Canonical Allele Identifier: CA040622

Gene: VHL

Linked Data

• ClinVar Variation Id: 386138
• ClinVar RCV Id: RCV000442110 ; RCV000476495 ; RCV001020243 ; RCV001143972
• dbSNP Id: rs372340900
• ExAC: 3:10188193 G / A
• gnomAD v2: 3-10188193-G-A
• gnomAD v3: 3-10146509-G-A
• gnomAD v4: 3-10146509-G-A
• MyVariant Identifiers: chr3:g.10188193G>A (hg19) ; chr3:g.10146509G>A (hg38)

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