Canonical Allele Identifier: CA2664399854

Gene: VHL

Linked Data

• gnomAD v4: 3-10141781-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141783_10141784del , CM000665.2:g.10141783_10141784del	GRCh38
NC_000003.11:g.10183467_10183468del , CM000665.1:g.10183467_10183468del	GRCh37
NC_000003.10:g.10158467_10158468del	NCBI36
NG_008212.3:g.5149_5150del , LRG_322:g.5149_5150del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696153.1:c.-65_-64del	ENSP00000512444.1:n.-65_-64del
ENST00000256474.3:c.-65_-64del MANE Select	ENSP00000256474.3:n.-65_-64del
ENST00000256474.2:c.-65_-64del	ENSP00000256474.2:n.-65_-64del
NM_000551.3:c.-65_-64del , LRG_322t1:c.-65_-64del	NP_000542.1:n.-65_-64del
NM_198156.2:c.-65_-64del	NP_937799.1:n.-65_-64del
XM_011534078.1:c.-65_-64del	XP_011532380.1:n.-65_-64del
NM_001354723.1:c.-65_-64del	NP_001341652.1:n.-65_-64del
NM_000551.4:c.-65_-64del MANE Select	NP_000542.1:n.-65_-64del
NM_001354723.2:c.-65_-64del	NP_001341652.1:n.-65_-64del
NM_198156.3:c.-65_-64del	NP_937799.1:n.-65_-64del