Canonical Allele Identifier: CA2664399921

Gene: VHL

Linked Data

• gnomAD v4: 3-10146680-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146681del , CM000665.2:g.10146681del	GRCh38
NC_000003.11:g.10188365del , CM000665.1:g.10188365del	GRCh37
NC_000003.10:g.10163365del	NCBI36
NG_008212.3:g.10047del , LRG_322:g.10047del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*140+45del	ENSP00000512434.1:n.*140+45del
ENST00000696143.1:c.600-3106del	ENSP00000512435.1:n.600-3106del
ENST00000696153.1:c.463+45del	ENSP00000512444.1:n.463+45del
ENST00000256474.3:c.463+45del MANE Select	ENSP00000256474.3:n.463+45del
ENST00000256474.2:c.463+45del	ENSP00000256474.2:n.463+45del
ENST00000345392.2:c.341-3106del	ENSP00000344757.2:n.341-3106del
ENST00000477538.1:n.599+45del
NM_000551.3:c.463+45del , LRG_322t1:c.463+45del	NP_000542.1:n.463+45del
NM_198156.2:c.341-3106del	NP_937799.1:n.341-3106del
NM_001354723.1:c.*18-3106del	NP_001341652.1:n.*18-3106del
NM_000551.4:c.463+45del MANE Select	NP_000542.1:n.463+45del
NM_001354723.2:c.*18-3106del	NP_001341652.1:n.*18-3106del
NM_198156.3:c.341-3106del	NP_937799.1:n.341-3106del