Canonical Allele Identifier: CA645524659
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM423173

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142021_10142027del , CM000665.2:g.10142021_10142027del GRCh38
NC_000003.11:g.10183705_10183711del , CM000665.1:g.10183705_10183711del GRCh37
NC_000003.10:g.10158705_10158711del NCBI36
NG_008212.3:g.5387_5393del , LRG_322:g.5387_5393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.174_180del ENSP00000512434.1:p.Arg60CysfsTer5
ENST00000696143.1:c.174_180del ENSP00000512435.1:p.Arg60CysfsTer5
ENST00000696153.1:c.174_180del ENSP00000512444.1:p.Arg60CysfsTer5
ENST00000256474.3:c.174_180del MANE Select ENSP00000256474.3:p.Arg60CysfsTer5
ENST00000256474.2:c.174_180del ENSP00000256474.2:p.Arg60CysfsTer5
ENST00000345392.2:c.174_180del ENSP00000344757.2:p.Arg60CysfsTer5
NM_000551.3:c.174_180del , LRG_322t1:c.174_180del NP_000542.1:p.Arg60CysfsTer5
NM_198156.2:c.174_180del NP_937799.1:p.Arg60CysfsTer5
XM_011534078.1:c.174_180del XP_011532380.1:p.Arg60CysfsTer5
NM_001354723.1:c.174_180del NP_001341652.1:p.Arg60CysfsTer5
NM_000551.4:c.174_180del MANE Select NP_000542.1:p.Arg60CysfsTer5
NM_001354723.2:c.174_180del NP_001341652.1:p.Arg60CysfsTer5
NM_198156.3:c.174_180del NP_937799.1:p.Arg60CysfsTer5