Canonical Allele Identifier: CA645524852

Gene: VHL

Linked Data

• COSMIC: COSM36338

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142178_10142183del , CM000665.2:g.10142178_10142183del	GRCh38
NC_000003.11:g.10183862_10183867del , CM000665.1:g.10183862_10183867del	GRCh37
NC_000003.10:g.10158862_10158867del	NCBI36
NG_008212.3:g.5544_5549del , LRG_322:g.5544_5549del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.331_336del	ENSP00000512434.1:p.Ser111_Tyr112del
ENST00000696143.1:c.331_336del	ENSP00000512435.1:p.Ser111_Tyr112del
ENST00000696153.1:c.331_336del	ENSP00000512444.1:p.Ser111_Tyr112del
ENST00000256474.3:c.331_336del MANE Select	ENSP00000256474.3:p.Ser111_Tyr112del
ENST00000256474.2:c.331_336del	ENSP00000256474.2:p.Ser111_Tyr112del
ENST00000345392.2:c.331_336del	ENSP00000344757.2:p.Ser111_Tyr112del
NM_000551.3:c.331_336del , LRG_322t1:c.331_336del	NP_000542.1:p.Ser111_Tyr112del
NM_198156.2:c.331_336del	NP_937799.1:p.Ser111_Tyr112del
XM_011534078.1:c.331_336del	XP_011532380.1:p.Ser111_Tyr112del
NM_001354723.1:c.331_336del	NP_001341652.1:p.Ser111_Tyr112del
NM_000551.4:c.331_336del MANE Select	NP_000542.1:p.Ser111_Tyr112del
NM_001354723.2:c.331_336del	NP_001341652.1:p.Ser111_Tyr112del
NM_198156.3:c.331_336del	NP_937799.1:p.Ser111_Tyr112del