Canonical Allele Identifier: CA3046517738
Community Standard Title: NM_000551.4(VHL):c.99_113del (p.Ala35_Gly39del)
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141946_10141960del , CM000665.2:g.10141946_10141960del GRCh38
NC_000003.11:g.10183630_10183644del , CM000665.1:g.10183630_10183644del GRCh37
NC_000003.10:g.10158630_10158644del NCBI36
NG_008212.3:g.5312_5326del , LRG_322:g.5312_5326del

Transcript Alleles

HGVS Amino-acid Change
NM_000551.4:c.99_113del MANE Select NP_000542.1:p.Gly34_Ser38del
ENST00000256474.3:c.99_113del MANE Select ENSP00000256474.3:p.Gly34_Ser38del
NM_000551.3:c.99_113del , LRG_322t1:c.99_113del NP_000542.1:p.Gly34_Ser38del
NM_001354723.1:c.99_113del NP_001341652.1:p.Gly34_Ser38del
NM_001354723.2:c.99_113del NP_001341652.1:p.Gly34_Ser38del
NM_198156.2:c.99_113del NP_937799.1:p.Gly34_Ser38del
NM_198156.3:c.99_113del NP_937799.1:p.Gly34_Ser38del
ENST00000256474.2:c.99_113del ENSP00000256474.2:p.Gly34_Ser38del
ENST00000345392.2:c.99_113del ENSP00000344757.2:p.Gly34_Ser38del
ENST00000696142.1:c.99_113del ENSP00000512434.1:p.Gly34_Ser38del
ENST00000696143.1:c.99_113del ENSP00000512435.1:p.Gly34_Ser38del
ENST00000696153.1:c.99_113del ENSP00000512444.1:p.Gly34_Ser38del
XM_011534078.1:c.99_113del XP_011532380.1:p.Gly34_Ser38del