Canonical Allele Identifier: CA1345058973

Gene: VHL

Linked Data

• ClinVar Variation Id: 2163126
• ClinVar RCV Id: RCV003073134
• dbSNP Id: rs143844761

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146656dup , CM000665.2:g.10146656dup	GRCh38
NC_000003.11:g.10188340dup , CM000665.1:g.10188340dup	GRCh37
NC_000003.10:g.10163340dup	NCBI36
NG_008212.3:g.10022dup , LRG_322:g.10022dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*140+20dup	ENSP00000512434.1:n.*140+20dup
ENST00000696143.1:c.600-3131dup	ENSP00000512435.1:n.600-3131dup
ENST00000696153.1:c.463+20dup	ENSP00000512444.1:n.463+20dup
ENST00000256474.3:c.463+20dup MANE Select	ENSP00000256474.3:n.463+20dup
ENST00000256474.2:c.463+20dup	ENSP00000256474.2:n.463+20dup
ENST00000345392.2:c.341-3131dup	ENSP00000344757.2:n.341-3131dup
ENST00000477538.1:n.599+20dup
NM_000551.3:c.463+20dup , LRG_322t1:c.463+20dup	NP_000542.1:n.463+20dup
NM_198156.2:c.341-3131dup	NP_937799.1:n.341-3131dup
NM_001354723.1:c.*18-3131dup	NP_001341652.1:n.*18-3131dup
NM_000551.4:c.463+20dup MANE Select	NP_000542.1:n.463+20dup
NM_001354723.2:c.*18-3131dup	NP_001341652.1:n.*18-3131dup
NM_198156.3:c.341-3131dup	NP_937799.1:n.341-3131dup