Canonical Allele Identifier: CA2695197690

Gene: VHL

Linked Data

• ClinVar Variation Id: 2674005
• ClinVar RCV Id: RCV003450606

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142106_10142107del , CM000665.2:g.10142106_10142107del	GRCh38
NC_000003.11:g.10183790_10183791del , CM000665.1:g.10183790_10183791del	GRCh37
NC_000003.10:g.10158790_10158791del	NCBI36
NG_008212.3:g.5472_5473del , LRG_322:g.5472_5473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.259_260del	ENSP00000512434.1:p.Val87MetfsTer?
ENST00000696143.1:c.259_260del	ENSP00000512435.1:p.Val87MetfsTer?
ENST00000696153.1:c.259_260del	ENSP00000512444.1:p.Val87MetfsTer?
ENST00000256474.3:c.259_260del MANE Select	ENSP00000256474.3:p.Val87MetfsTer?
ENST00000256474.2:c.259_260del	ENSP00000256474.2:p.Val87MetfsTer?
ENST00000345392.2:c.259_260del	ENSP00000344757.2:p.Val87MetfsTer?
NM_000551.3:c.259_260del , LRG_322t1:c.259_260del	NP_000542.1:p.Val87MetfsTer?
NM_198156.2:c.259_260del	NP_937799.1:p.Val87MetfsTer?
XM_011534078.1:c.259_260del	XP_011532380.1:p.Val87MetfsTer?
NM_001354723.1:c.259_260del	NP_001341652.1:p.Val87MetfsTer?
NM_000551.4:c.259_260del MANE Select	NP_000542.1:p.Val87MetfsTer?
NM_001354723.2:c.259_260del	NP_001341652.1:p.Val87MetfsTer?
NM_198156.3:c.259_260del	NP_937799.1:p.Val87MetfsTer?