Canonical Allele Identifier: CA351754066

Gene: VHL

Linked Data

• dbSNP Id: rs2125128387
• MyVariant Identifiers: chr3:g.10188267T>A (hg19) ; chr3:g.10146583T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146583T>A , CM000665.2:g.10146583T>A	GRCh38
NC_000003.11:g.10188267T>A , CM000665.1:g.10188267T>A	GRCh37
NC_000003.10:g.10163267T>A	NCBI36
NG_008212.3:g.9949T>A , LRG_322:g.9949T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*87T>A	ENSP00000512434.1:n.*87T>A
ENST00000696143.1:c.600-3204T>A	ENSP00000512435.1:n.600-3204T>A
ENST00000696153.1:c.410T>A	ENSP00000512444.1:p.Val137Glu
ENST00000256474.3:c.410T>A MANE Select	ENSP00000256474.3:p.Val137Glu
ENST00000256474.2:c.410T>A	ENSP00000256474.2:p.Val137Glu
ENST00000345392.2:c.341-3204T>A	ENSP00000344757.2:n.341-3204T>A
ENST00000477538.1:n.546T>A
NM_000551.3:c.410T>A , LRG_322t1:c.410T>A	NP_000542.1:p.Val137Glu
NM_198156.2:c.341-3204T>A	NP_937799.1:n.341-3204T>A
XM_011534078.1:c.*87T>A	XP_011532380.1:n.*87T>A
NM_001354723.1:c.*18-3204T>A	NP_001341652.1:n.*18-3204T>A
NM_000551.4:c.410T>A MANE Select	NP_000542.1:p.Val137Glu
NM_001354723.2:c.*18-3204T>A	NP_001341652.1:n.*18-3204T>A
NM_198156.3:c.341-3204T>A	NP_937799.1:n.341-3204T>A