Canonical Allele Identifier: CA1805592891

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99121170T= , CM000670.2:g.99121170T=	GRCh38
NC_000008.10:g.100133398T= , CM000670.1:g.100133398T=	GRCh37
NC_000008.9:g.100202574T=	NCBI36
NG_007098.2:g.112905T= , LRG_351:g.112905T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355155.6:c.938-7T=	ENSP00000347281.2:n.938-7T=
ENST00000682145.1:n.1007-7T=
ENST00000682153.1:c.938-7T=	ENSP00000507923.1:n.938-7T=
ENST00000682234.1:c.938-7T=	ENSP00000508225.1:n.938-7T=
ENST00000682358.1:n.1008-7T=
ENST00000682853.1:n.1158-7T=
ENST00000683334.1:c.938-7T=	ENSP00000507369.1:n.938-7T=
ENST00000683486.1:n.1004-7T=
ENST00000683619.1:n.1041-7T=
ENST00000683869.1:n.1019-7T=
ENST00000684269.1:n.1039-7T=
ENST00000684308.1:n.1004-7T=
ENST00000357162.7:c.938-7T= MANE Select	ENSP00000349685.2:n.938-7T=
ENST00000358544.7:c.938-7T= MANE Plus Clinical	ENSP00000351346.2:n.938-7T=
ENST00000355155.5:c.938-7T=	ENSP00000347281.1:n.938-7T=
ENST00000357162.6:c.938-7T=	ENSP00000349685.2:n.938-7T=
ENST00000358544.6:c.938-7T=	ENSP00000351346.2:n.938-7T=
ENST00000441350.2:c.938-7T=	ENSP00000398472.2:n.938-7T=
ENST00000496144.5:c.938-7T=	ENSP00000430900.1:n.938-7T=
ENST00000524330.1:n.63-7T=
NM_015243.2:c.938-7T= , LRG_351t3:c.938-7T=	NP_056058.2:n.938-7T=
NM_017890.4:c.938-7T= , LRG_351t1:c.938-7T=	NP_060360.3:n.938-7T=
NM_152564.4:c.938-7T= , LRG_351t2:c.938-7T=	NP_689777.3:n.938-7T=
NM_181661.2:c.938-7T= , LRG_351t4:c.938-7T=	NP_858047.2:n.938-7T=
NR_047582.1:n.1164-7T=
XM_005250800.2:c.938-7T=	XP_005250857.1:n.938-7T=
XM_005250801.3:c.938-7T=	XP_005250858.1:n.938-7T=
XM_006716510.2:c.938-7T=	XP_006716573.1:n.938-7T=
XM_006716511.2:c.938-7T=	XP_006716574.1:n.938-7T=
XM_011516848.1:c.938-7T=	XP_011515150.1:n.938-7T=
XM_011516849.1:c.938-7T=	XP_011515151.1:n.938-7T=
XM_011516850.1:c.560-7T=	XP_011515152.1:n.560-7T=
XM_011516853.1:c.938-7T=	XP_011515155.1:n.938-7T=
XM_011516855.1:c.938-7T=	XP_011515157.1:n.938-7T=
XM_011516856.1:c.938-7T=	XP_011515158.1:n.938-7T=
XM_011516857.1:c.938-7T=	XP_011515159.1:n.938-7T=
XM_011516858.1:c.938-7T=	XP_011515160.1:n.938-7T=
XM_011516859.1:c.938-7T=	XP_011515161.1:n.938-7T=
XM_011516860.1:c.938-7T=	XP_011515162.1:n.938-7T=
XM_011516861.1:c.938-7T=	XP_011515163.1:n.938-7T=
XM_011516862.1:c.938-7T=	XP_011515164.1:n.938-7T=
XM_011516863.1:c.938-7T=	XP_011515165.1:n.938-7T=
XM_011516864.1:c.938-7T=	XP_011515166.1:n.938-7T=
XM_011516865.1:c.938-7T=	XP_011515167.1:n.938-7T=
XM_011516866.1:c.938-7T=	XP_011515168.1:n.938-7T=
XR_928301.1:n.1041-7T=
XR_928302.1:n.1041-7T=
XR_928303.1:n.1041-7T=
XR_928304.1:n.1041-7T=
XM_005250800.3:c.938-7T=	XP_005250857.1:n.938-7T=
XM_005250801.5:c.938-7T=	XP_005250858.1:n.938-7T=
XM_006716510.3:c.938-7T=	XP_006716573.1:n.938-7T=
XM_011516848.2:c.938-7T=	XP_011515150.1:n.938-7T=
XM_011516849.2:c.938-7T=	XP_011515151.1:n.938-7T=
XM_011516850.2:c.560-7T=	XP_011515152.1:n.560-7T=
XM_011516853.2:c.938-7T=	XP_011515155.1:n.938-7T=
XM_011516859.2:c.938-7T=	XP_011515161.1:n.938-7T=
XM_011516866.2:c.938-7T=	XP_011515168.1:n.938-7T=
XM_017013109.1:c.938-7T=	XP_016868598.1:n.938-7T=
XM_024447074.1:c.-390-7T=	XP_024302842.1:n.-390-7T=
XM_024447075.1:c.938-7T=	XP_024302843.1:n.938-7T=
XR_001745481.1:n.1041-7T=
XR_001745482.2:n.1041-7T=
XR_001745484.2:n.1041-7T=
XR_002956601.1:n.1041-7T=
XR_002956602.1:n.1041-7T=
XR_928302.2:n.1041-7T=
NM_015243.3:c.938-7T=	NP_056058.2:n.938-7T=
NM_017890.5:c.938-7T= MANE Plus Clinical	NP_060360.3:n.938-7T=
NM_152564.5:c.938-7T= MANE Select	NP_689777.3:n.938-7T=
NM_181661.3:c.938-7T=	NP_858047.2:n.938-7T=
NR_047582.2:n.1156-7T=