Canonical Allele Identifier: CA2664400149

Gene: VHL

Linked Data

• gnomAD v4: 3-10150142-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150142G>A , CM000665.2:g.10150142G>A	GRCh38
NC_000003.11:g.10191826G>A , CM000665.1:g.10191826G>A	GRCh37
NC_000003.10:g.10166826G>A	NCBI36
NG_008212.3:g.13508G>A , LRG_322:g.13508G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*496G>A	ENSP00000512434.1:n.*496G>A
ENST00000696143.1:c.955G>A	ENSP00000512435.1:n.955G>A
ENST00000696153.1:c.*177G>A	ENSP00000512444.1:n.*177G>A
ENST00000256474.3:c.*177G>A MANE Select	ENSP00000256474.3:n.*177G>A
ENST00000256474.2:c.*177G>A	ENSP00000256474.2:n.*177G>A
ENST00000345392.2:c.*177G>A	ENSP00000344757.2:n.*177G>A
ENST00000477538.1:n.955G>A
NM_000551.3:c.*177G>A , LRG_322t1:c.*177G>A	NP_000542.1:n.*177G>A
NM_198156.2:c.*177G>A	NP_937799.1:n.*177G>A
NM_001354723.1:c.*373G>A	NP_001341652.1:n.*373G>A
NM_000551.4:c.*177G>A MANE Select	NP_000542.1:n.*177G>A
NM_001354723.2:c.*373G>A	NP_001341652.1:n.*373G>A
NM_198156.3:c.*177G>A	NP_937799.1:n.*177G>A