Canonical Allele Identifier: CA658655621
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142143_10142155del , CM000665.2:g.10142143_10142155del GRCh38
NC_000003.11:g.10183827_10183839del , CM000665.1:g.10183827_10183839del GRCh37
NC_000003.10:g.10158827_10158839del NCBI36
NG_008212.3:g.5509_5521del , LRG_322:g.5509_5521del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.296_308del ENSP00000512434.1:p.Pro99LeufsTer14
ENST00000696143.1:c.296_308del ENSP00000512435.1:p.Pro99LeufsTer14
ENST00000696153.1:c.296_308del ENSP00000512444.1:p.Pro99LeufsTer?
ENST00000256474.3:c.296_308del MANE Select ENSP00000256474.3:p.Pro99LeufsTer?
ENST00000256474.2:c.296_308del ENSP00000256474.2:p.Pro99LeufsTer?
ENST00000345392.2:c.296_308del ENSP00000344757.2:p.Pro99LeufsTer15
NM_000551.3:c.296_308del , LRG_322t1:c.296_308del NP_000542.1:p.Pro99LeufsTer?
NM_198156.2:c.296_308del NP_937799.1:p.Pro99LeufsTer15
XM_011534078.1:c.296_308del XP_011532380.1:p.Pro99LeufsTer14
NM_001354723.1:c.296_308del NP_001341652.1:p.Pro99LeufsTer14
NM_000551.4:c.296_308del MANE Select NP_000542.1:p.Pro99LeufsTer?
NM_001354723.2:c.296_308del NP_001341652.1:p.Pro99LeufsTer14
NM_198156.3:c.296_308del NP_937799.1:p.Pro99LeufsTer15