Canonical Allele Identifier: CA351756211

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191524G>A (hg19) ; chr3:g.10149840G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149840G>A , CM000665.2:g.10149840G>A	GRCh38
NC_000003.11:g.10191524G>A , CM000665.1:g.10191524G>A	GRCh37
NC_000003.10:g.10166524G>A	NCBI36
NG_008212.3:g.13206G>A , LRG_322:g.13206G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*194G>A	ENSP00000512434.1:n.*194G>A
ENST00000696143.1:c.653G>A	ENSP00000512435.1:n.653G>A
ENST00000696153.1:c.628G>A	ENSP00000512444.1:p.Glu210Lys
ENST00000256474.3:c.517G>A MANE Select	ENSP00000256474.3:p.Glu173Lys
ENST00000256474.2:c.517G>A	ENSP00000256474.2:p.Glu173Lys
ENST00000345392.2:c.394G>A	ENSP00000344757.2:p.Glu132Lys
ENST00000477538.1:n.653G>A
NM_000551.3:c.517G>A , LRG_322t1:c.517G>A	NP_000542.1:p.Glu173Lys
NM_198156.2:c.394G>A	NP_937799.1:p.Glu132Lys
NM_001354723.1:c.*71G>A	NP_001341652.1:n.*71G>A
NM_000551.4:c.517G>A MANE Select	NP_000542.1:p.Glu173Lys
NM_001354723.2:c.*71G>A	NP_001341652.1:n.*71G>A
NM_198156.3:c.394G>A	NP_937799.1:p.Glu132Lys