Canonical Allele Identifier: CA2516248721

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99819188_99819189del , CM000670.2:g.99819188_99819189del	GRCh38
NC_000008.10:g.100831416_100831417del , CM000670.1:g.100831416_100831417del	GRCh37
NC_000008.9:g.100900592_100900593del	NCBI36
NG_007098.2:g.810923_810924del , LRG_351:g.810923_810924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8697-224_8697-223del	ENSP00000507923.1:n.8697-224_8697-223del
ENST00000682358.1:n.8767-224_8767-223del
ENST00000683334.1:c.*4379-224_*4379-223del	ENSP00000507369.1:n.*4379-224_*4379-223del
ENST00000357162.7:c.8622-224_8622-223del MANE Select	ENSP00000349685.2:n.8622-224_8622-223del
ENST00000358544.7:c.8697-224_8697-223del MANE Plus Clinical	ENSP00000351346.2:n.8697-224_8697-223del
ENST00000357162.6:c.8622-224_8622-223del	ENSP00000349685.2:n.8622-224_8622-223del
ENST00000358544.6:c.8697-224_8697-223del	ENSP00000351346.2:n.8697-224_8697-223del
NM_017890.4:c.8697-224_8697-223del , LRG_351t1:c.8697-224_8697-223del	NP_060360.3:n.8697-224_8697-223del
NM_152564.4:c.8622-224_8622-223del , LRG_351t2:c.8622-224_8622-223del	NP_689777.3:n.8622-224_8622-223del
XM_005250800.2:c.8697-224_8697-223del	XP_005250857.1:n.8697-224_8697-223del
XM_005250801.3:c.8697-224_8697-223del	XP_005250858.1:n.8697-224_8697-223del
XM_011516848.1:c.8694-224_8694-223del	XP_011515150.1:n.8694-224_8694-223del
XM_011516849.1:c.8619-224_8619-223del	XP_011515151.1:n.8619-224_8619-223del
XM_011516850.1:c.8319-224_8319-223del	XP_011515152.1:n.8319-224_8319-223del
XM_011516851.1:c.5583-224_5583-223del	XP_011515153.1:n.5583-224_5583-223del
XM_011516852.1:c.5583-224_5583-223del	XP_011515154.1:n.5583-224_5583-223del
XM_011516854.1:c.4476-224_4476-223del	XP_011515156.1:n.4476-224_4476-223del
XM_005250800.3:c.8697-224_8697-223del	XP_005250857.1:n.8697-224_8697-223del
XM_005250801.5:c.8697-224_8697-223del	XP_005250858.1:n.8697-224_8697-223del
XM_011516848.2:c.8694-224_8694-223del	XP_011515150.1:n.8694-224_8694-223del
XM_011516849.2:c.8619-224_8619-223del	XP_011515151.1:n.8619-224_8619-223del
XM_011516850.2:c.8319-224_8319-223del	XP_011515152.1:n.8319-224_8319-223del
XM_011516851.2:c.5583-224_5583-223del	XP_011515153.1:n.5583-224_5583-223del
XM_011516852.2:c.5583-224_5583-223del	XP_011515154.1:n.5583-224_5583-223del
XM_011516854.2:c.4476-224_4476-223del	XP_011515156.1:n.4476-224_4476-223del
XM_017013109.1:c.8502-224_8502-223del	XP_016868598.1:n.8502-224_8502-223del
XM_017013111.1:c.5583-224_5583-223del	XP_016868600.1:n.5583-224_5583-223del
XM_017013112.1:c.4254-224_4254-223del	XP_016868601.1:n.4254-224_4254-223del
XM_024447074.1:c.7482-224_7482-223del	XP_024302842.1:n.7482-224_7482-223del
NM_017890.5:c.8697-224_8697-223del MANE Plus Clinical	NP_060360.3:n.8697-224_8697-223del
NM_152564.5:c.8622-224_8622-223del MANE Select	NP_689777.3:n.8622-224_8622-223del