Canonical Allele Identifier: CA645524934

Gene: VHL

Linked Data

• COSMIC: COSM17613

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146572_10146573del , CM000665.2:g.10146572_10146573del	GRCh38
NC_000003.11:g.10188256_10188257del , CM000665.1:g.10188256_10188257del	GRCh37
NC_000003.10:g.10163256_10163257del	NCBI36
NG_008212.3:g.9938_9939del , LRG_322:g.9938_9939del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*76_*77del	ENSP00000512434.1:n.*76_*77del
ENST00000696143.1:c.600-3215_600-3214del	ENSP00000512435.1:n.600-3215_600-3214del
ENST00000696153.1:c.399_400del	ENSP00000512444.1:p.Glu134IlefsTer9
ENST00000256474.3:c.399_400del MANE Select	ENSP00000256474.3:p.Glu134IlefsTer9
ENST00000256474.2:c.399_400del	ENSP00000256474.2:p.Glu134IlefsTer9
ENST00000345392.2:c.341-3215_341-3214del	ENSP00000344757.2:n.341-3215_341-3214del
ENST00000477538.1:n.535_536del
NM_000551.3:c.399_400del , LRG_322t1:c.399_400del	NP_000542.1:p.Glu134IlefsTer9
NM_198156.2:c.341-3215_341-3214del	NP_937799.1:n.341-3215_341-3214del
XM_011534078.1:c.*76_*77del	XP_011532380.1:n.*76_*77del
NM_001354723.1:c.*18-3215_*18-3214del	NP_001341652.1:n.*18-3215_*18-3214del
NM_000551.4:c.399_400del MANE Select	NP_000542.1:p.Glu134IlefsTer9
NM_001354723.2:c.*18-3215_*18-3214del	NP_001341652.1:n.*18-3215_*18-3214del
NM_198156.3:c.341-3215_341-3214del	NP_937799.1:n.341-3215_341-3214del