Canonical Allele Identifier: CA1805715052
Gene: VPS13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99391575C= , CM000670.2:g.99391575C= GRCh38
NC_000008.10:g.100403803C= , CM000670.1:g.100403803C= GRCh37
NC_000008.9:g.100472979C= NCBI36
NG_007098.2:g.383310C= , LRG_351:g.383310C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355155.6:c.2950C= ENSP00000347281.2:p.Pro984=
ENST00000682145.1:n.2830C=
ENST00000682153.1:c.2953C= ENSP00000507923.1:p.Pro985=
ENST00000682234.1:c.2953C= ENSP00000508225.1:p.Pro985=
ENST00000682358.1:n.3023C=
ENST00000683334.1:c.2953C= ENSP00000507369.1:p.Pro985=
ENST00000683486.1:n.3019C=
ENST00000683619.1:n.3125C=
ENST00000683869.1:n.3034C=
ENST00000357162.7:c.2953C= MANE Select ENSP00000349685.2:p.Pro985=
ENST00000358544.7:c.2953C= MANE Plus Clinical ENSP00000351346.2:p.Pro985=
ENST00000357162.6:c.2953C= ENSP00000349685.2:p.Pro985=
ENST00000358544.6:c.2953C= ENSP00000351346.2:p.Pro985=
ENST00000496144.5:c.2953C= ENSP00000430900.1:p.Pro985=
ENST00000521037.1:n.124C=
ENST00000522802.5:n.175C=
NM_017890.4:c.2953C= , LRG_351t1:c.2953C= NP_060360.3:p.Pro985=
NM_152564.4:c.2953C= , LRG_351t2:c.2953C= NP_689777.3:p.Pro985=
XM_005250800.2:c.2953C= XP_005250857.1:p.Pro985=
XM_005250801.3:c.2953C= XP_005250858.1:p.Pro985=
XM_006716510.2:c.2953C= XP_006716573.1:p.Pro985=
XM_011516848.1:c.2950C= XP_011515150.1:p.Pro984=
XM_011516849.1:c.2953C= XP_011515151.1:p.Pro985=
XM_011516850.1:c.2575C= XP_011515152.1:p.Pro859=
XM_011516853.1:c.2953C= XP_011515155.1:p.Pro985=
XM_011516855.1:c.2953C= XP_011515157.1:p.Pro985=
XM_011516856.1:c.2953C= XP_011515158.1:p.Pro985=
XM_011516857.1:c.2953C= XP_011515159.1:p.Pro985=
XM_011516858.1:c.2953C= XP_011515160.1:p.Pro985=
XM_011516859.1:c.2953C= XP_011515161.1:p.Pro985=
XM_011516860.1:c.2953C= XP_011515162.1:p.Pro985=
XM_011516861.1:c.2953C= XP_011515163.1:p.Pro985=
XR_928301.1:n.3056C=
XR_928302.1:n.3056C=
XR_928303.1:n.3056C=
XR_928304.1:n.3056C=
XM_005250800.3:c.2953C= XP_005250857.1:p.Pro985=
XM_005250801.5:c.2953C= XP_005250858.1:p.Pro985=
XM_006716510.3:c.2953C= XP_006716573.1:p.Pro985=
XM_011516848.2:c.2950C= XP_011515150.1:p.Pro984=
XM_011516849.2:c.2953C= XP_011515151.1:p.Pro985=
XM_011516850.2:c.2575C= XP_011515152.1:p.Pro859=
XM_011516853.2:c.2953C= XP_011515155.1:p.Pro985=
XM_011516859.2:c.2953C= XP_011515161.1:p.Pro985=
XM_017013109.1:c.2758C= XP_016868598.1:p.Pro920=
XM_024447074.1:c.1738C= XP_024302842.1:p.Pro580=
XM_024447075.1:c.2953C= XP_024302843.1:p.Pro985=
XR_001745481.1:n.3056C=
XR_001745482.2:n.3056C=
XR_001745484.2:n.3056C=
XR_002956601.1:n.3053C=
XR_002956602.1:n.3056C=
XR_928302.2:n.3056C=
NM_017890.5:c.2953C= MANE Plus Clinical NP_060360.3:p.Pro985=
NM_152564.5:c.2953C= MANE Select NP_689777.3:p.Pro985=