Canonical Allele Identifier: CA351756592

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191609T>G (hg19) ; chr3:g.10149925T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149925T>G , CM000665.2:g.10149925T>G	GRCh38
NC_000003.11:g.10191609T>G , CM000665.1:g.10191609T>G	GRCh37
NC_000003.10:g.10166609T>G	NCBI36
NG_008212.3:g.13291T>G , LRG_322:g.13291T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*279T>G	ENSP00000512434.1:n.*279T>G
ENST00000696143.1:c.738T>G	ENSP00000512435.1:n.738T>G
ENST00000696153.1:c.713T>G	ENSP00000512444.1:p.Leu238Arg
ENST00000256474.3:c.602T>G MANE Select	ENSP00000256474.3:p.Leu201Arg
ENST00000256474.2:c.602T>G	ENSP00000256474.2:p.Leu201Arg
ENST00000345392.2:c.479T>G	ENSP00000344757.2:p.Leu160Arg
ENST00000477538.1:n.738T>G
NM_000551.3:c.602T>G , LRG_322t1:c.602T>G	NP_000542.1:p.Leu201Arg
NM_198156.2:c.479T>G	NP_937799.1:p.Leu160Arg
NM_001354723.1:c.*156T>G	NP_001341652.1:n.*156T>G
NM_000551.4:c.602T>G MANE Select	NP_000542.1:p.Leu201Arg
NM_001354723.2:c.*156T>G	NP_001341652.1:n.*156T>G
NM_198156.3:c.479T>G	NP_937799.1:p.Leu160Arg