Canonical Allele Identifier: CA2688064914

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99391513-GAAAAACT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99391526_99391532del , CM000670.2:g.99391526_99391532del	GRCh38
NC_000008.10:g.100403754_100403760del , CM000670.1:g.100403754_100403760del	GRCh37
NC_000008.9:g.100472930_100472936del	NCBI36
NG_007098.2:g.383261_383267del , LRG_351:g.383261_383267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355155.6:c.2935-34_2935-28del	ENSP00000347281.2:n.2935-34_2935-28del
ENST00000682145.1:n.2812-31_2812-25del
ENST00000682153.1:c.2935-31_2935-25del	ENSP00000507923.1:n.2935-31_2935-25del
ENST00000682234.1:c.2935-31_2935-25del	ENSP00000508225.1:n.2935-31_2935-25del
ENST00000682358.1:n.3005-31_3005-25del
ENST00000683334.1:c.2935-31_2935-25del	ENSP00000507369.1:n.2935-31_2935-25del
ENST00000683486.1:n.3001-31_3001-25del
ENST00000683619.1:n.3107-31_3107-25del
ENST00000683869.1:n.3016-31_3016-25del
ENST00000357162.7:c.2935-31_2935-25del MANE Select	ENSP00000349685.2:n.2935-31_2935-25del
ENST00000358544.7:c.2935-31_2935-25del MANE Plus Clinical	ENSP00000351346.2:n.2935-31_2935-25del
ENST00000357162.6:c.2935-31_2935-25del	ENSP00000349685.2:n.2935-31_2935-25del
ENST00000358544.6:c.2935-31_2935-25del	ENSP00000351346.2:n.2935-31_2935-25del
ENST00000496144.5:c.2935-31_2935-25del	ENSP00000430900.1:n.2935-31_2935-25del
ENST00000521037.1:n.106-31_106-25del
ENST00000522802.5:n.157-31_157-25del
NM_017890.4:c.2935-31_2935-25del , LRG_351t1:c.2935-31_2935-25del	NP_060360.3:n.2935-31_2935-25del
NM_152564.4:c.2935-31_2935-25del , LRG_351t2:c.2935-31_2935-25del	NP_689777.3:n.2935-31_2935-25del
XM_005250800.2:c.2935-31_2935-25del	XP_005250857.1:n.2935-31_2935-25del
XM_005250801.3:c.2935-31_2935-25del	XP_005250858.1:n.2935-31_2935-25del
XM_006716510.2:c.2935-31_2935-25del	XP_006716573.1:n.2935-31_2935-25del
XM_011516848.1:c.2935-34_2935-28del	XP_011515150.1:n.2935-34_2935-28del
XM_011516849.1:c.2935-31_2935-25del	XP_011515151.1:n.2935-31_2935-25del
XM_011516850.1:c.2557-31_2557-25del	XP_011515152.1:n.2557-31_2557-25del
XM_011516853.1:c.2935-31_2935-25del	XP_011515155.1:n.2935-31_2935-25del
XM_011516855.1:c.2935-31_2935-25del	XP_011515157.1:n.2935-31_2935-25del
XM_011516856.1:c.2935-31_2935-25del	XP_011515158.1:n.2935-31_2935-25del
XM_011516857.1:c.2935-31_2935-25del	XP_011515159.1:n.2935-31_2935-25del
XM_011516858.1:c.2935-31_2935-25del	XP_011515160.1:n.2935-31_2935-25del
XM_011516859.1:c.2935-31_2935-25del	XP_011515161.1:n.2935-31_2935-25del
XM_011516860.1:c.2935-31_2935-25del	XP_011515162.1:n.2935-31_2935-25del
XM_011516861.1:c.2935-31_2935-25del	XP_011515163.1:n.2935-31_2935-25del
XR_928301.1:n.3038-31_3038-25del
XR_928302.1:n.3038-31_3038-25del
XR_928303.1:n.3038-31_3038-25del
XR_928304.1:n.3038-31_3038-25del
XM_005250800.3:c.2935-31_2935-25del	XP_005250857.1:n.2935-31_2935-25del
XM_005250801.5:c.2935-31_2935-25del	XP_005250858.1:n.2935-31_2935-25del
XM_006716510.3:c.2935-31_2935-25del	XP_006716573.1:n.2935-31_2935-25del
XM_011516848.2:c.2935-34_2935-28del	XP_011515150.1:n.2935-34_2935-28del
XM_011516849.2:c.2935-31_2935-25del	XP_011515151.1:n.2935-31_2935-25del
XM_011516850.2:c.2557-31_2557-25del	XP_011515152.1:n.2557-31_2557-25del
XM_011516853.2:c.2935-31_2935-25del	XP_011515155.1:n.2935-31_2935-25del
XM_011516859.2:c.2935-31_2935-25del	XP_011515161.1:n.2935-31_2935-25del
XM_017013109.1:c.2740-31_2740-25del	XP_016868598.1:n.2740-31_2740-25del
XM_024447074.1:c.1720-31_1720-25del	XP_024302842.1:n.1720-31_1720-25del
XM_024447075.1:c.2935-31_2935-25del	XP_024302843.1:n.2935-31_2935-25del
XR_001745481.1:n.3038-31_3038-25del
XR_001745482.2:n.3038-31_3038-25del
XR_001745484.2:n.3038-31_3038-25del
XR_002956601.1:n.3038-34_3038-28del
XR_002956602.1:n.3038-31_3038-25del
XR_928302.2:n.3038-31_3038-25del
NM_017890.5:c.2935-31_2935-25del MANE Plus Clinical	NP_060360.3:n.2935-31_2935-25del
NM_152564.5:c.2935-31_2935-25del MANE Select	NP_689777.3:n.2935-31_2935-25del