Canonical Allele Identifier: CA351756074

Gene: VHL

Linked Data

• COSMIC: COSM30286
• MyVariant Identifiers: chr3:g.10191480T>G (hg19) ; chr3:g.10149796T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149796T>G , CM000665.2:g.10149796T>G	GRCh38
NC_000003.11:g.10191480T>G , CM000665.1:g.10191480T>G	GRCh37
NC_000003.10:g.10166480T>G	NCBI36
NG_008212.3:g.13162T>G , LRG_322:g.13162T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*150T>G	ENSP00000512434.1:n.*150T>G
ENST00000696143.1:c.609T>G	ENSP00000512435.1:n.609T>G
ENST00000696153.1:c.584T>G	ENSP00000512444.1:p.Leu195Arg
ENST00000256474.3:c.473T>G MANE Select	ENSP00000256474.3:p.Leu158Arg
ENST00000256474.2:c.473T>G	ENSP00000256474.2:p.Leu158Arg
ENST00000345392.2:c.350T>G	ENSP00000344757.2:p.Leu117Arg
ENST00000477538.1:n.609T>G
NM_000551.3:c.473T>G , LRG_322t1:c.473T>G	NP_000542.1:p.Leu158Arg
NM_198156.2:c.350T>G	NP_937799.1:p.Leu117Arg
NM_001354723.1:c.*27T>G	NP_001341652.1:n.*27T>G
NM_000551.4:c.473T>G MANE Select	NP_000542.1:p.Leu158Arg
NM_001354723.2:c.*27T>G	NP_001341652.1:n.*27T>G
NM_198156.3:c.350T>G	NP_937799.1:p.Leu117Arg