Canonical Allele Identifier: CA020365

Gene: VHL

Linked Data

• ClinVar Variation Id: 36903
• ClinVar RCV Id: RCV000030587 ; RCV001022748
• dbSNP Id: rs193922611
• COSMIC: COSM1738373
• MyVariant Identifiers: chr3:g.10188315T>A (hg19) ; chr3:g.10146631T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146631T>A , CM000665.2:g.10146631T>A	GRCh38
NC_000003.11:g.10188315T>A , CM000665.1:g.10188315T>A	GRCh37
NC_000003.10:g.10163315T>A	NCBI36
NG_008212.3:g.9997T>A , LRG_322:g.9997T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*135T>A	ENSP00000512434.1:n.*135T>A
ENST00000696143.1:c.600-3156T>A	ENSP00000512435.1:n.600-3156T>A
ENST00000696153.1:c.458T>A	ENSP00000512444.1:p.Leu153Gln
ENST00000256474.3:c.458T>A MANE Select	ENSP00000256474.3:p.Leu153Gln
ENST00000256474.2:c.458T>A	ENSP00000256474.2:p.Leu153Gln
ENST00000345392.2:c.341-3156T>A	ENSP00000344757.2:n.341-3156T>A
ENST00000477538.1:n.594T>A
NM_000551.3:c.458T>A , LRG_322t1:c.458T>A	NP_000542.1:p.Leu153Gln
NM_198156.2:c.341-3156T>A	NP_937799.1:n.341-3156T>A
NM_001354723.1:c.*18-3156T>A	NP_001341652.1:n.*18-3156T>A
NM_000551.4:c.458T>A MANE Select	NP_000542.1:p.Leu153Gln
NM_001354723.2:c.*18-3156T>A	NP_001341652.1:n.*18-3156T>A
NM_198156.3:c.341-3156T>A	NP_937799.1:n.341-3156T>A