Canonical Allele Identifier: CA1805614133

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99192806_99192807delinsAG , CM000670.2:g.99192806_99192807delinsAG	GRCh38
NC_000008.10:g.100205034_100205035delinsAG , CM000670.1:g.100205034_100205035delinsAG	GRCh37
NC_000008.9:g.100274210_100274211delinsAG	NCBI36
NG_007098.2:g.184541_184542delinsAG , LRG_351:g.184541_184542delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000355155.6:c.2334-70_2334-69delinsAG	ENSP00000347281.2:n.2334-70_2334-69delins...
ENST00000682145.1:n.2211-70_2211-69delinsAG
ENST00000682153.1:c.2334-70_2334-69delinsAG	ENSP00000507923.1:n.2334-70_2334-69delins...
ENST00000682234.1:c.2334-70_2334-69delinsAG	ENSP00000508225.1:n.2334-70_2334-69delins...
ENST00000682358.1:n.2404-70_2404-69delinsAG
ENST00000682853.1:n.2554-70_2554-69delinsAG
ENST00000683334.1:c.2334-70_2334-69delinsAG	ENSP00000507369.1:n.2334-70_2334-69delins...
ENST00000683486.1:n.2400-70_2400-69delinsAG
ENST00000683619.1:n.2506-70_2506-69delinsAG
ENST00000683869.1:n.2415-70_2415-69delinsAG
ENST00000684308.1:n.2400-70_2400-69delinsAG
ENST00000357162.7:c.2334-70_2334-69delinsAG MANE Select	ENSP00000349685.2:n.2334-70_2334-69delins...
ENST00000358544.7:c.2334-70_2334-69delinsAG MANE Plus Clinical	ENSP00000351346.2:n.2334-70_2334-69delins...
ENST00000355155.5:c.2334-70_2334-69delinsAG	ENSP00000347281.1:n.2334-70_2334-69delins...
ENST00000357162.6:c.2334-70_2334-69delinsAG	ENSP00000349685.2:n.2334-70_2334-69delins...
ENST00000358544.6:c.2334-70_2334-69delinsAG	ENSP00000351346.2:n.2334-70_2334-69delins...
ENST00000496144.5:c.2334-70_2334-69delinsAG	ENSP00000430900.1:n.2334-70_2334-69delins...
ENST00000521932.1:n.241-70_241-69delinsAG
NM_015243.2:c.2334-70_2334-69delinsAG , LRG_351t3:c.2334-70_2334-69delinsAG	NP_056058.2:n.2334-70_2334-69delinsAG
NM_017890.4:c.2334-70_2334-69delinsAG , LRG_351t1:c.2334-70_2334-69delinsAG	NP_060360.3:n.2334-70_2334-69delinsAG
NM_152564.4:c.2334-70_2334-69delinsAG , LRG_351t2:c.2334-70_2334-69delinsAG	NP_689777.3:n.2334-70_2334-69delinsAG
XM_005250800.2:c.2334-70_2334-69delinsAG	XP_005250857.1:n.2334-70_2334-69delinsAG
XM_005250801.3:c.2334-70_2334-69delinsAG	XP_005250858.1:n.2334-70_2334-69delinsAG
XM_006716510.2:c.2334-70_2334-69delinsAG	XP_006716573.1:n.2334-70_2334-69delinsAG
XM_006716511.2:c.2334-70_2334-69delinsAG	XP_006716574.1:n.2334-70_2334-69delinsAG
XM_011516848.1:c.2334-70_2334-69delinsAG	XP_011515150.1:n.2334-70_2334-69delinsAG
XM_011516849.1:c.2334-70_2334-69delinsAG	XP_011515151.1:n.2334-70_2334-69delinsAG
XM_011516850.1:c.1956-70_1956-69delinsAG	XP_011515152.1:n.1956-70_1956-69delinsAG
XM_011516853.1:c.2334-70_2334-69delinsAG	XP_011515155.1:n.2334-70_2334-69delinsAG
XM_011516855.1:c.2334-70_2334-69delinsAG	XP_011515157.1:n.2334-70_2334-69delinsAG
XM_011516856.1:c.2334-70_2334-69delinsAG	XP_011515158.1:n.2334-70_2334-69delinsAG
XM_011516857.1:c.2334-70_2334-69delinsAG	XP_011515159.1:n.2334-70_2334-69delinsAG
XM_011516858.1:c.2334-70_2334-69delinsAG	XP_011515160.1:n.2334-70_2334-69delinsAG
XM_011516859.1:c.2334-70_2334-69delinsAG	XP_011515161.1:n.2334-70_2334-69delinsAG
XM_011516860.1:c.2334-70_2334-69delinsAG	XP_011515162.1:n.2334-70_2334-69delinsAG
XM_011516861.1:c.2334-70_2334-69delinsAG	XP_011515163.1:n.2334-70_2334-69delinsAG
XM_011516862.1:c.2334-70_2334-69delinsAG	XP_011515164.1:n.2334-70_2334-69delinsAG
XM_011516863.1:c.2334-70_2334-69delinsAG	XP_011515165.1:n.2334-70_2334-69delinsAG
XM_011516864.1:c.2334-70_2334-69delinsAG	XP_011515166.1:n.2334-70_2334-69delinsAG
XM_011516865.1:c.2334-70_2334-69delinsAG	XP_011515167.1:n.2334-70_2334-69delinsAG
XM_011516866.1:c.2334-70_2334-69delinsAG	XP_011515168.1:n.2334-70_2334-69delinsAG
XR_928301.1:n.2437-70_2437-69delinsAG
XR_928302.1:n.2437-70_2437-69delinsAG
XR_928303.1:n.2437-70_2437-69delinsAG
XR_928304.1:n.2437-70_2437-69delinsAG
XM_005250800.3:c.2334-70_2334-69delinsAG	XP_005250857.1:n.2334-70_2334-69delinsAG
XM_005250801.5:c.2334-70_2334-69delinsAG	XP_005250858.1:n.2334-70_2334-69delinsAG
XM_006716510.3:c.2334-70_2334-69delinsAG	XP_006716573.1:n.2334-70_2334-69delinsAG
XM_011516848.2:c.2334-70_2334-69delinsAG	XP_011515150.1:n.2334-70_2334-69delinsAG
XM_011516849.2:c.2334-70_2334-69delinsAG	XP_011515151.1:n.2334-70_2334-69delinsAG
XM_011516850.2:c.1956-70_1956-69delinsAG	XP_011515152.1:n.1956-70_1956-69delinsAG
XM_011516853.2:c.2334-70_2334-69delinsAG	XP_011515155.1:n.2334-70_2334-69delinsAG
XM_011516859.2:c.2334-70_2334-69delinsAG	XP_011515161.1:n.2334-70_2334-69delinsAG
XM_011516866.2:c.2334-70_2334-69delinsAG	XP_011515168.1:n.2334-70_2334-69delinsAG
XM_017013109.1:c.2139-70_2139-69delinsAG	XP_016868598.1:n.2139-70_2139-69delinsAG
XM_024447074.1:c.1119-70_1119-69delinsAG	XP_024302842.1:n.1119-70_1119-69delinsAG
XM_024447075.1:c.2334-70_2334-69delinsAG	XP_024302843.1:n.2334-70_2334-69delinsAG
XR_001745481.1:n.2437-70_2437-69delinsAG
XR_001745482.2:n.2437-70_2437-69delinsAG
XR_001745484.2:n.2437-70_2437-69delinsAG
XR_002956601.1:n.2437-70_2437-69delinsAG
XR_002956602.1:n.2437-70_2437-69delinsAG
XR_928302.2:n.2437-70_2437-69delinsAG
NM_015243.3:c.2334-70_2334-69delinsAG	NP_056058.2:n.2334-70_2334-69delinsAG
NM_017890.5:c.2334-70_2334-69delinsAG MANE Plus Clinical	NP_060360.3:n.2334-70_2334-69delinsAG
NM_152564.5:c.2334-70_2334-69delinsAG MANE Select	NP_689777.3:n.2334-70_2334-69delinsAG