Canonical Allele Identifier: CA645524812
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM27566

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142134_10142138del , CM000665.2:g.10142134_10142138del GRCh38
NC_000003.11:g.10183818_10183822del , CM000665.1:g.10183818_10183822del GRCh37
NC_000003.10:g.10158818_10158822del NCBI36
NG_008212.3:g.5500_5504del , LRG_322:g.5500_5504del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.287_291del ENSP00000512434.1:p.Gln96LeufsTer?
ENST00000696143.1:c.287_291del ENSP00000512435.1:p.Gln96LeufsTer?
ENST00000696153.1:c.287_291del ENSP00000512444.1:p.Gln96LeufsTer?
ENST00000256474.3:c.287_291del MANE Select ENSP00000256474.3:p.Gln96LeufsTer?
ENST00000256474.2:c.287_291del ENSP00000256474.2:p.Gln96LeufsTer?
ENST00000345392.2:c.287_291del ENSP00000344757.2:p.Gln96LeufsTer?
NM_000551.3:c.287_291del , LRG_322t1:c.287_291del NP_000542.1:p.Gln96LeufsTer?
NM_198156.2:c.287_291del NP_937799.1:p.Gln96LeufsTer?
XM_011534078.1:c.287_291del XP_011532380.1:p.Gln96LeufsTer?
NM_001354723.1:c.287_291del NP_001341652.1:p.Gln96LeufsTer?
NM_000551.4:c.287_291del MANE Select NP_000542.1:p.Gln96LeufsTer?
NM_001354723.2:c.287_291del NP_001341652.1:p.Gln96LeufsTer?
NM_198156.3:c.287_291del NP_937799.1:p.Gln96LeufsTer?