Canonical Allele Identifier: CA645524753

Gene: VHL

Linked Data

• COSMIC: COSM17720

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142086_10142088del , CM000665.2:g.10142086_10142088del	GRCh38
NC_000003.11:g.10183770_10183772del , CM000665.1:g.10183770_10183772del	GRCh37
NC_000003.10:g.10158770_10158772del	NCBI36
NG_008212.3:g.5452_5454del , LRG_322:g.5452_5454del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.239_241del	ENSP00000512434.1:p.Ser80_Pro81delinsThr
ENST00000696143.1:c.239_241del	ENSP00000512435.1:p.Ser80_Pro81delinsThr
ENST00000696153.1:c.239_241del	ENSP00000512444.1:p.Ser80_Pro81delinsThr
ENST00000256474.3:c.239_241del MANE Select	ENSP00000256474.3:p.Ser80_Pro81delinsThr
ENST00000256474.2:c.239_241del	ENSP00000256474.2:p.Ser80_Pro81delinsThr
ENST00000345392.2:c.239_241del	ENSP00000344757.2:p.Ser80_Pro81delinsThr
NM_000551.3:c.239_241del , LRG_322t1:c.239_241del	NP_000542.1:p.Ser80_Pro81delinsThr
NM_198156.2:c.239_241del	NP_937799.1:p.Ser80_Pro81delinsThr
XM_011534078.1:c.239_241del	XP_011532380.1:p.Ser80_Pro81delinsThr
NM_001354723.1:c.239_241del	NP_001341652.1:p.Ser80_Pro81delinsThr
NM_000551.4:c.239_241del MANE Select	NP_000542.1:p.Ser80_Pro81delinsThr
NM_001354723.2:c.239_241del	NP_001341652.1:p.Ser80_Pro81delinsThr
NM_198156.3:c.239_241del	NP_937799.1:p.Ser80_Pro81delinsThr