Canonical Allele Identifier: CA351756116

Gene: VHL

Linked Data

• dbSNP Id: rs1553620313
• MyVariant Identifiers: chr3:g.10191491T>G (hg19) ; chr3:g.10149807T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149807T>G , CM000665.2:g.10149807T>G	GRCh38
NC_000003.11:g.10191491T>G , CM000665.1:g.10191491T>G	GRCh37
NC_000003.10:g.10166491T>G	NCBI36
NG_008212.3:g.13173T>G , LRG_322:g.13173T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*161T>G	ENSP00000512434.1:n.*161T>G
ENST00000696143.1:c.620T>G	ENSP00000512435.1:n.620T>G
ENST00000696153.1:c.595T>G	ENSP00000512444.1:p.Cys199Gly
ENST00000256474.3:c.484T>G MANE Select	ENSP00000256474.3:p.Cys162Gly
ENST00000256474.2:c.484T>G	ENSP00000256474.2:p.Cys162Gly
ENST00000345392.2:c.361T>G	ENSP00000344757.2:p.Cys121Gly
ENST00000477538.1:n.620T>G
NM_000551.3:c.484T>G , LRG_322t1:c.484T>G	NP_000542.1:p.Cys162Gly
NM_198156.2:c.361T>G	NP_937799.1:p.Cys121Gly
NM_001354723.1:c.*38T>G	NP_001341652.1:n.*38T>G
NM_000551.4:c.484T>G MANE Select	NP_000542.1:p.Cys162Gly
NM_001354723.2:c.*38T>G	NP_001341652.1:n.*38T>G
NM_198156.3:c.361T>G	NP_937799.1:p.Cys121Gly