Canonical Allele Identifier: CA2781480155

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99832780_99832794del , CM000670.2:g.99832780_99832794del	GRCh38
NC_000008.10:g.100845008_100845022del , CM000670.1:g.100845008_100845022del	GRCh37
NC_000008.9:g.100914184_100914198del	NCBI36
NG_007098.2:g.824515_824529del , LRG_351:g.824515_824529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.9689+128_9689+142del	ENSP00000507923.1:n.9689+128_9689+142del
ENST00000682358.1:n.9759+128_9759+142del
ENST00000683334.1:c.*5371+128_*5371+142del	ENSP00000507369.1:n.*5371+128_*5371+142del
ENST00000357162.7:c.9614+128_9614+142del MANE Select	ENSP00000349685.2:n.9614+128_9614+142del
ENST00000358544.7:c.9689+128_9689+142del MANE Plus Clinical	ENSP00000351346.2:n.9689+128_9689+142del
ENST00000357162.6:c.9614+128_9614+142del	ENSP00000349685.2:n.9614+128_9614+142del
ENST00000358544.6:c.9689+128_9689+142del	ENSP00000351346.2:n.9689+128_9689+142del
NM_017890.4:c.9689+128_9689+142del , LRG_351t1:c.9689+128_9689+142del	NP_060360.3:n.9689+128_9689+142del
NM_152564.4:c.9614+128_9614+142del , LRG_351t2:c.9614+128_9614+142del	NP_689777.3:n.9614+128_9614+142del
XM_005250800.2:c.9689+128_9689+142del	XP_005250857.1:n.9689+128_9689+142del
XM_005250801.3:c.9689+128_9689+142del	XP_005250858.1:n.9689+128_9689+142del
XM_011516848.1:c.9686+128_9686+142del	XP_011515150.1:n.9686+128_9686+142del
XM_011516849.1:c.9611+128_9611+142del	XP_011515151.1:n.9611+128_9611+142del
XM_011516850.1:c.9311+128_9311+142del	XP_011515152.1:n.9311+128_9311+142del
XM_011516851.1:c.6575+128_6575+142del	XP_011515153.1:n.6575+128_6575+142del
XM_011516852.1:c.6575+128_6575+142del	XP_011515154.1:n.6575+128_6575+142del
XM_011516854.1:c.5468+128_5468+142del	XP_011515156.1:n.5468+128_5468+142del
XM_005250800.3:c.9689+128_9689+142del	XP_005250857.1:n.9689+128_9689+142del
XM_005250801.5:c.9689+128_9689+142del	XP_005250858.1:n.9689+128_9689+142del
XM_011516848.2:c.9686+128_9686+142del	XP_011515150.1:n.9686+128_9686+142del
XM_011516849.2:c.9611+128_9611+142del	XP_011515151.1:n.9611+128_9611+142del
XM_011516850.2:c.9311+128_9311+142del	XP_011515152.1:n.9311+128_9311+142del
XM_011516851.2:c.6575+128_6575+142del	XP_011515153.1:n.6575+128_6575+142del
XM_011516852.2:c.6575+128_6575+142del	XP_011515154.1:n.6575+128_6575+142del
XM_011516854.2:c.5468+128_5468+142del	XP_011515156.1:n.5468+128_5468+142del
XM_017013109.1:c.9494+128_9494+142del	XP_016868598.1:n.9494+128_9494+142del
XM_017013111.1:c.6575+128_6575+142del	XP_016868600.1:n.6575+128_6575+142del
XM_017013112.1:c.5246+128_5246+142del	XP_016868601.1:n.5246+128_5246+142del
XM_024447074.1:c.8474+128_8474+142del	XP_024302842.1:n.8474+128_8474+142del
NM_017890.5:c.9689+128_9689+142del MANE Plus Clinical	NP_060360.3:n.9689+128_9689+142del
NM_152564.5:c.9614+128_9614+142del MANE Select	NP_689777.3:n.9614+128_9614+142del