Canonical Allele Identifier: CA70049452
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs5030649

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146557del , CM000665.2:g.10146557del GRCh38
NC_000003.11:g.10188241del , CM000665.1:g.10188241del GRCh37
NC_000003.10:g.10163241del NCBI36
NG_008212.3:g.9923del , LRG_322:g.9923del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*61del ENSP00000512434.1:n.*61del
ENST00000696143.1:c.600-3230del ENSP00000512435.1:n.600-3230del
ENST00000696153.1:c.384del ENSP00000512444.1:p.Leu129TrpfsTer?
ENST00000256474.3:c.384del MANE Select ENSP00000256474.3:p.Leu129TrpfsTer?
ENST00000256474.2:c.384del ENSP00000256474.2:p.Leu129TrpfsTer?
ENST00000345392.2:c.341-3230del ENSP00000344757.2:n.341-3230del
ENST00000477538.1:n.520del
NM_000551.3:c.384del , LRG_322t1:c.384del NP_000542.1:p.Leu129TrpfsTer?
NM_198156.2:c.341-3230del NP_937799.1:n.341-3230del
XM_011534078.1:c.*61del XP_011532380.1:n.*61del
NM_001354723.1:c.*18-3230del NP_001341652.1:n.*18-3230del
NM_000551.4:c.384del MANE Select NP_000542.1:p.Leu129TrpfsTer?
NM_001354723.2:c.*18-3230del NP_001341652.1:n.*18-3230del
NM_198156.3:c.341-3230del NP_937799.1:n.341-3230del