Canonical Allele Identifier: CA182328557

Gene: VPS13B

Linked Data

• dbSNP Id: rs756168442
• gnomAD v4: 8-99819333-TAG-T
• MyVariant Identifiers: chr8:g.100831562_100831563del (hg19) ; chr8:g.99819334_99819335del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99819334_99819335del , CM000670.2:g.99819334_99819335del	GRCh38
NC_000008.10:g.100831562_100831563del , CM000670.1:g.100831562_100831563del	GRCh37
NC_000008.9:g.100900738_100900739del	NCBI36
NG_007098.2:g.811069_811070del , LRG_351:g.811069_811070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8697-78_8697-77del	ENSP00000507923.1:n.8697-78_8697-77del
ENST00000682358.1:n.8767-78_8767-77del
ENST00000683334.1:c.*4379-78_*4379-77del	ENSP00000507369.1:n.*4379-78_*4379-77del
ENST00000357162.7:c.8622-78_8622-77del MANE Select	ENSP00000349685.2:n.8622-78_8622-77del
ENST00000358544.7:c.8697-78_8697-77del MANE Plus Clinical	ENSP00000351346.2:n.8697-78_8697-77del
ENST00000357162.6:c.8622-78_8622-77del	ENSP00000349685.2:n.8622-78_8622-77del
ENST00000358544.6:c.8697-78_8697-77del	ENSP00000351346.2:n.8697-78_8697-77del
NM_017890.4:c.8697-78_8697-77del , LRG_351t1:c.8697-78_8697-77del	NP_060360.3:n.8697-78_8697-77del
NM_152564.4:c.8622-78_8622-77del , LRG_351t2:c.8622-78_8622-77del	NP_689777.3:n.8622-78_8622-77del
XM_005250800.2:c.8697-78_8697-77del	XP_005250857.1:n.8697-78_8697-77del
XM_005250801.3:c.8697-78_8697-77del	XP_005250858.1:n.8697-78_8697-77del
XM_011516848.1:c.8694-78_8694-77del	XP_011515150.1:n.8694-78_8694-77del
XM_011516849.1:c.8619-78_8619-77del	XP_011515151.1:n.8619-78_8619-77del
XM_011516850.1:c.8319-78_8319-77del	XP_011515152.1:n.8319-78_8319-77del
XM_011516851.1:c.5583-78_5583-77del	XP_011515153.1:n.5583-78_5583-77del
XM_011516852.1:c.5583-78_5583-77del	XP_011515154.1:n.5583-78_5583-77del
XM_011516854.1:c.4476-78_4476-77del	XP_011515156.1:n.4476-78_4476-77del
XM_005250800.3:c.8697-78_8697-77del	XP_005250857.1:n.8697-78_8697-77del
XM_005250801.5:c.8697-78_8697-77del	XP_005250858.1:n.8697-78_8697-77del
XM_011516848.2:c.8694-78_8694-77del	XP_011515150.1:n.8694-78_8694-77del
XM_011516849.2:c.8619-78_8619-77del	XP_011515151.1:n.8619-78_8619-77del
XM_011516850.2:c.8319-78_8319-77del	XP_011515152.1:n.8319-78_8319-77del
XM_011516851.2:c.5583-78_5583-77del	XP_011515153.1:n.5583-78_5583-77del
XM_011516852.2:c.5583-78_5583-77del	XP_011515154.1:n.5583-78_5583-77del
XM_011516854.2:c.4476-78_4476-77del	XP_011515156.1:n.4476-78_4476-77del
XM_017013109.1:c.8502-78_8502-77del	XP_016868598.1:n.8502-78_8502-77del
XM_017013111.1:c.5583-78_5583-77del	XP_016868600.1:n.5583-78_5583-77del
XM_017013112.1:c.4254-78_4254-77del	XP_016868601.1:n.4254-78_4254-77del
XM_024447074.1:c.7482-78_7482-77del	XP_024302842.1:n.7482-78_7482-77del
NM_017890.5:c.8697-78_8697-77del MANE Plus Clinical	NP_060360.3:n.8697-78_8697-77del
NM_152564.5:c.8622-78_8622-77del MANE Select	NP_689777.3:n.8622-78_8622-77del