Canonical Allele Identifier: CA645524912

Gene: VHL

Linked Data

• COSMIC: COSM4186742

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146548del , CM000665.2:g.10146548del	GRCh38
NC_000003.11:g.10188232del , CM000665.1:g.10188232del	GRCh37
NC_000003.10:g.10163232del	NCBI36
NG_008212.3:g.9914del , LRG_322:g.9914del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*52del	ENSP00000512434.1:n.*52del
ENST00000696143.1:c.600-3239del	ENSP00000512435.1:n.600-3239del
ENST00000696153.1:c.375del	ENSP00000512444.1:p.His125GlnfsTer?
ENST00000256474.3:c.375del MANE Select	ENSP00000256474.3:p.His125GlnfsTer?
ENST00000256474.2:c.375del	ENSP00000256474.2:p.His125GlnfsTer?
ENST00000345392.2:c.341-3239del	ENSP00000344757.2:n.341-3239del
ENST00000477538.1:n.511del
NM_000551.3:c.375del , LRG_322t1:c.375del	NP_000542.1:p.His125GlnfsTer?
NM_198156.2:c.341-3239del	NP_937799.1:n.341-3239del
XM_011534078.1:c.*52del	XP_011532380.1:n.*52del
NM_001354723.1:c.*18-3239del	NP_001341652.1:n.*18-3239del
NM_000551.4:c.375del MANE Select	NP_000542.1:p.His125GlnfsTer?
NM_001354723.2:c.*18-3239del	NP_001341652.1:n.*18-3239del
NM_198156.3:c.341-3239del	NP_937799.1:n.341-3239del