Canonical Allele Identifier: CA2580068444

Gene: VHL

Linked Data

• ClinVar Variation Id: 1948434
• ClinVar RCV Id: RCV002685756

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142942del , CM000665.2:g.10142942del	GRCh38
NC_000003.11:g.10184626del , CM000665.1:g.10184626del	GRCh37
NC_000003.10:g.10159626del	NCBI36
NG_008212.3:g.6308del , LRG_322:g.6308del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.520del	ENSP00000512434.1:p.Cys174AlafsTer23
ENST00000696143.1:c.520del	ENSP00000512435.1:p.Cys174AlafsTer23
ENST00000696153.1:c.340+755del	ENSP00000512444.1:n.340+755del
ENST00000256474.3:c.340+755del MANE Select	ENSP00000256474.3:n.340+755del
ENST00000256474.2:c.340+755del	ENSP00000256474.2:n.340+755del
ENST00000345392.2:c.340+755del	ENSP00000344757.2:n.340+755del
ENST00000477538.1:n.397del
NM_000551.3:c.340+755del , LRG_322t1:c.340+755del	NP_000542.1:n.340+755del
NM_198156.2:c.340+755del	NP_937799.1:n.340+755del
XM_011534078.1:c.520del	XP_011532380.1:p.Cys174AlafsTer23
NM_001354723.1:c.520del	NP_001341652.1:p.Cys174AlafsTer23
NM_000551.4:c.340+755del MANE Select	NP_000542.1:n.340+755del
NM_001354723.2:c.520del	NP_001341652.1:p.Cys174AlafsTer23
NM_198156.3:c.340+755del	NP_937799.1:n.340+755del