Canonical Allele Identifier: CA2573136139

Gene: VHL

Linked Data

• ClinVar Variation Id: 1464433
• ClinVar RCV Id: RCV001956887
• dbSNP Id: rs2125126091

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142974C>A , CM000665.2:g.10142974C>A	GRCh38
NC_000003.11:g.10184658C>A , CM000665.1:g.10184658C>A	GRCh37
NC_000003.10:g.10159658C>A	NCBI36
NG_008212.3:g.6340C>A , LRG_322:g.6340C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.552C>A	ENSP00000512434.1:p.Phe184Leu
ENST00000696143.1:c.552C>A	ENSP00000512435.1:p.Phe184Leu
ENST00000696153.1:c.340+787C>A	ENSP00000512444.1:n.340+787C>A
ENST00000256474.3:c.340+787C>A MANE Select	ENSP00000256474.3:n.340+787C>A
ENST00000256474.2:c.340+787C>A	ENSP00000256474.2:n.340+787C>A
ENST00000345392.2:c.340+787C>A	ENSP00000344757.2:n.340+787C>A
ENST00000477538.1:n.429C>A
NM_000551.3:c.340+787C>A , LRG_322t1:c.340+787C>A	NP_000542.1:n.340+787C>A
NM_198156.2:c.340+787C>A	NP_937799.1:n.340+787C>A
XM_011534078.1:c.552C>A	XP_011532380.1:p.Phe184Leu
NM_001354723.1:c.552C>A	NP_001341652.1:p.Phe184Leu
NM_000551.4:c.340+787C>A MANE Select	NP_000542.1:n.340+787C>A
NM_001354723.2:c.552C>A	NP_001341652.1:p.Phe184Leu
NM_198156.3:c.340+787C>A	NP_937799.1:n.340+787C>A