Canonical Allele Identifier: CA284769
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 68080
dbSNP Id: rs180177371

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99853770_99853771del , CM000670.2:g.99853770_99853771del GRCh38
NC_000008.10:g.100865998_100865999del , CM000670.1:g.100865998_100865999del GRCh37
NC_000008.9:g.100935174_100935175del NCBI36
NG_007098.2:g.845505_845506del , LRG_351:g.845505_845506del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682153.1:c.10456_10457del ENSP00000507923.1:p.Leu3487ProfsTer24
ENST00000682358.1:n.10526_10527del
ENST00000683334.1:c.*6138_*6139del ENSP00000507369.1:n.*6138_*6139del
ENST00000357162.7:c.10381_10382del MANE Select ENSP00000349685.2:p.Leu3462ProfsTer24
ENST00000358544.7:c.10456_10457del MANE Plus Clinical ENSP00000351346.2:p.Leu3487ProfsTer24
ENST00000357162.6:c.10381_10382del ENSP00000349685.2:p.Leu3462ProfsTer24
ENST00000358544.6:c.10456_10457del ENSP00000351346.2:p.Leu3487ProfsTer24
NM_017890.4:c.10456_10457del , LRG_351t1:c.10456_10457del NP_060360.3:p.Leu3487ProfsTer24
NM_152564.4:c.10381_10382del , LRG_351t2:c.10381_10382del NP_689777.3:p.Leu3462ProfsTer24
XM_005250800.2:c.10456_10457del XP_005250857.1:p.Leu3487ProfsTer24
XM_005250801.3:c.10456_10457del XP_005250858.1:p.Leu3487ProfsTer24
XM_011516848.1:c.10453_10454del XP_011515150.1:p.Leu3486ProfsTer24
XM_011516849.1:c.10378_10379del XP_011515151.1:p.Leu3461ProfsTer24
XM_011516850.1:c.10078_10079del XP_011515152.1:p.Leu3361ProfsTer24
XM_011516851.1:c.7342_7343del XP_011515153.1:p.Leu2449ProfsTer24
XM_011516852.1:c.7342_7343del XP_011515154.1:p.Leu2449ProfsTer24
XM_011516854.1:c.6235_6236del XP_011515156.1:p.Leu2080ProfsTer24
XM_005250800.3:c.10456_10457del XP_005250857.1:p.Leu3487ProfsTer24
XM_005250801.5:c.10456_10457del XP_005250858.1:p.Leu3487ProfsTer24
XM_011516848.2:c.10453_10454del XP_011515150.1:p.Leu3486ProfsTer24
XM_011516849.2:c.10378_10379del XP_011515151.1:p.Leu3461ProfsTer24
XM_011516850.2:c.10078_10079del XP_011515152.1:p.Leu3361ProfsTer24
XM_011516851.2:c.7342_7343del XP_011515153.1:p.Leu2449ProfsTer24
XM_011516852.2:c.7342_7343del XP_011515154.1:p.Leu2449ProfsTer24
XM_011516854.2:c.6235_6236del XP_011515156.1:p.Leu2080ProfsTer24
XM_017013109.1:c.10261_10262del XP_016868598.1:p.Leu3422ProfsTer24
XM_017013111.1:c.7342_7343del XP_016868600.1:p.Leu2449ProfsTer24
XM_017013112.1:c.6013_6014del XP_016868601.1:p.Leu2006ProfsTer24
XM_024447074.1:c.9241_9242del XP_024302842.1:p.Leu3082ProfsTer24
NM_017890.5:c.10456_10457del MANE Plus Clinical NP_060360.3:p.Leu3487ProfsTer24
NM_152564.5:c.10381_10382del MANE Select NP_689777.3:p.Leu3462ProfsTer24