Canonical Allele Identifier: CA351754317

Gene: VHL

Linked Data

• ClinVar Variation Id: 1018515
• ClinVar RCV Id: RCV001317824
• dbSNP Id: rs1696266503
• MyVariant Identifiers: chr3:g.10188303C>T (hg19) ; chr3:g.10146619C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146619C>T , CM000665.2:g.10146619C>T	GRCh38
NC_000003.11:g.10188303C>T , CM000665.1:g.10188303C>T	GRCh37
NC_000003.10:g.10163303C>T	NCBI36
NG_008212.3:g.9985C>T , LRG_322:g.9985C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*123C>T	ENSP00000512434.1:n.*123C>T
ENST00000696143.1:c.600-3168C>T	ENSP00000512435.1:n.600-3168C>T
ENST00000696153.1:c.446C>T	ENSP00000512444.1:p.Ala149Val
ENST00000256474.3:c.446C>T MANE Select	ENSP00000256474.3:p.Ala149Val
ENST00000256474.2:c.446C>T	ENSP00000256474.2:p.Ala149Val
ENST00000345392.2:c.341-3168C>T	ENSP00000344757.2:n.341-3168C>T
ENST00000477538.1:n.582C>T
NM_000551.3:c.446C>T , LRG_322t1:c.446C>T	NP_000542.1:p.Ala149Val
NM_198156.2:c.341-3168C>T	NP_937799.1:n.341-3168C>T
NM_001354723.1:c.*18-3168C>T	NP_001341652.1:n.*18-3168C>T
NM_000551.4:c.446C>T MANE Select	NP_000542.1:p.Ala149Val
NM_001354723.2:c.*18-3168C>T	NP_001341652.1:n.*18-3168C>T
NM_198156.3:c.341-3168C>T	NP_937799.1:n.341-3168C>T