Canonical Allele Identifier: CA2740090899

Gene: VHL

Linked Data

• ClinVar Variation Id: 2947050
• ClinVar RCV Id: RCV003801240

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141954_10141961del , CM000665.2:g.10141954_10141961del	GRCh38
NC_000003.11:g.10183638_10183645del , CM000665.1:g.10183638_10183645del	GRCh37
NC_000003.10:g.10158638_10158645del	NCBI36
NG_008212.3:g.5320_5327del , LRG_322:g.5320_5327del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.107_114del	ENSP00000512434.1:p.Glu36GlyfsTer?
ENST00000696143.1:c.107_114del	ENSP00000512435.1:p.Glu36GlyfsTer?
ENST00000696153.1:c.107_114del	ENSP00000512444.1:p.Glu36GlyfsTer?
ENST00000256474.3:c.107_114del MANE Select	ENSP00000256474.3:p.Glu36GlyfsTer?
ENST00000256474.2:c.107_114del	ENSP00000256474.2:p.Glu36GlyfsTer?
ENST00000345392.2:c.107_114del	ENSP00000344757.2:p.Glu36GlyfsTer?
NM_000551.3:c.107_114del , LRG_322t1:c.107_114del	NP_000542.1:p.Glu36GlyfsTer?
NM_198156.2:c.107_114del	NP_937799.1:p.Glu36GlyfsTer?
XM_011534078.1:c.107_114del	XP_011532380.1:p.Glu36GlyfsTer?
NM_001354723.1:c.107_114del	NP_001341652.1:p.Glu36GlyfsTer?
NM_000551.4:c.107_114del MANE Select	NP_000542.1:p.Glu36GlyfsTer?
NM_001354723.2:c.107_114del	NP_001341652.1:p.Glu36GlyfsTer?
NM_198156.3:c.107_114del	NP_937799.1:p.Glu36GlyfsTer?