Canonical Allele Identifier: CA70047555

Gene: VHL

Linked Data

• dbSNP Id: rs969804092
• gnomAD v3: 3-10143796-A-T
• gnomAD v4: 3-10143796-A-T
• MyVariant Identifiers: chr3:g.10185480A>T (hg19) ; chr3:g.10143796A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10143796A>T , CM000665.2:g.10143796A>T	GRCh38
NC_000003.11:g.10185480A>T , CM000665.1:g.10185480A>T	GRCh37
NC_000003.10:g.10160480A>T	NCBI36
NG_008212.3:g.7162A>T , LRG_322:g.7162A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*17+775A>T	ENSP00000512434.1:n.*17+775A>T
ENST00000696143.1:c.599+775A>T	ENSP00000512435.1:n.599+775A>T
ENST00000696153.1:c.340+1609A>T	ENSP00000512444.1:n.340+1609A>T
ENST00000256474.3:c.340+1609A>T MANE Select	ENSP00000256474.3:n.340+1609A>T
ENST00000256474.2:c.340+1609A>T	ENSP00000256474.2:n.340+1609A>T
ENST00000345392.2:c.340+1609A>T	ENSP00000344757.2:n.340+1609A>T
ENST00000477538.1:n.476+775A>T
NM_000551.3:c.340+1609A>T , LRG_322t1:c.340+1609A>T	NP_000542.1:n.340+1609A>T
NM_198156.2:c.340+1609A>T	NP_937799.1:n.340+1609A>T
XM_011534078.1:c.*17+775A>T	XP_011532380.1:n.*17+775A>T
NM_001354723.1:c.*17+775A>T	NP_001341652.1:n.*17+775A>T
NM_000551.4:c.340+1609A>T MANE Select	NP_000542.1:n.340+1609A>T
NM_001354723.2:c.*17+775A>T	NP_001341652.1:n.*17+775A>T
NM_198156.3:c.340+1609A>T	NP_937799.1:n.340+1609A>T