Canonical Allele Identifier: CA2695196567

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142117_10142118del , CM000665.2:g.10142117_10142118del	GRCh38
NC_000003.11:g.10183801_10183802del , CM000665.1:g.10183801_10183802del	GRCh37
NC_000003.10:g.10158801_10158802del	NCBI36
NG_008212.3:g.5483_5484del , LRG_322:g.5483_5484del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.270_271del	ENSP00000512434.1:p.Phe91ArgfsTer?
ENST00000696143.1:c.270_271del	ENSP00000512435.1:p.Phe91ArgfsTer?
ENST00000696153.1:c.270_271del	ENSP00000512444.1:p.Phe91ArgfsTer?
ENST00000256474.3:c.270_271del MANE Select	ENSP00000256474.3:p.Phe91ArgfsTer?
ENST00000256474.2:c.270_271del	ENSP00000256474.2:p.Phe91ArgfsTer?
ENST00000345392.2:c.270_271del	ENSP00000344757.2:p.Phe91ArgfsTer?
NM_000551.3:c.270_271del , LRG_322t1:c.270_271del	NP_000542.1:p.Phe91ArgfsTer?
NM_198156.2:c.270_271del	NP_937799.1:p.Phe91ArgfsTer?
XM_011534078.1:c.270_271del	XP_011532380.1:p.Phe91ArgfsTer?
NM_001354723.1:c.270_271del	NP_001341652.1:p.Phe91ArgfsTer?
NM_000551.4:c.270_271del MANE Select	NP_000542.1:p.Phe91ArgfsTer?
NM_001354723.2:c.270_271del	NP_001341652.1:p.Phe91ArgfsTer?
NM_198156.3:c.270_271del	NP_937799.1:p.Phe91ArgfsTer?