Canonical Allele Identifier: CA4825215

Gene: VPS13B

Linked Data

• dbSNP Id: rs747637077
• ExAC: 8:100880668 T / C
• gnomAD v2: 8-100880668-T-C
• MyVariant Identifiers: chr8:g.100880668T>C (hg19) ; chr8:g.99868440T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868440T>C , CM000670.2:g.99868440T>C	GRCh38
NC_000008.10:g.100880668T>C , CM000670.1:g.100880668T>C	GRCh37
NC_000008.9:g.100949844T>C	NCBI36
NG_007098.2:g.860175T>C , LRG_351:g.860175T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*536T>C	ENSP00000507923.1:n.*536T>C
ENST00000682358.1:n.11512T>C
ENST00000683334.1:c.*7124T>C	ENSP00000507369.1:n.*7124T>C
ENST00000357162.7:c.11367T>C MANE Select	ENSP00000349685.2:p.Ala3789=
ENST00000358544.7:c.11442T>C MANE Plus Clinical	ENSP00000351346.2:p.Ala3814=
ENST00000357162.6:c.11367T>C	ENSP00000349685.2:p.Ala3789=
ENST00000358544.6:c.11442T>C	ENSP00000351346.2:p.Ala3814=
ENST00000493587.1:n.384T>C
NM_017890.4:c.11442T>C , LRG_351t1:c.11442T>C	NP_060360.3:p.Ala3814=
NM_152564.4:c.11367T>C , LRG_351t2:c.11367T>C	NP_689777.3:p.Ala3789=
XM_005250800.2:c.11442T>C	XP_005250857.1:p.Ala3814=
XM_005250801.3:c.11442T>C	XP_005250858.1:p.Ala3814=
XM_011516848.1:c.11439T>C	XP_011515150.1:p.Ala3813=
XM_011516849.1:c.11364T>C	XP_011515151.1:p.Ala3788=
XM_011516850.1:c.11064T>C	XP_011515152.1:p.Ala3688=
XM_011516851.1:c.8328T>C	XP_011515153.1:p.Ala2776=
XM_011516852.1:c.8328T>C	XP_011515154.1:p.Ala2776=
XM_011516854.1:c.7221T>C	XP_011515156.1:p.Ala2407=
XM_005250800.3:c.11442T>C	XP_005250857.1:p.Ala3814=
XM_005250801.5:c.11442T>C	XP_005250858.1:p.Ala3814=
XM_011516848.2:c.11439T>C	XP_011515150.1:p.Ala3813=
XM_011516849.2:c.11364T>C	XP_011515151.1:p.Ala3788=
XM_011516850.2:c.11064T>C	XP_011515152.1:p.Ala3688=
XM_011516851.2:c.8328T>C	XP_011515153.1:p.Ala2776=
XM_011516852.2:c.8328T>C	XP_011515154.1:p.Ala2776=
XM_011516854.2:c.7221T>C	XP_011515156.1:p.Ala2407=
XM_017013109.1:c.11247T>C	XP_016868598.1:p.Ala3749=
XM_017013111.1:c.8328T>C	XP_016868600.1:p.Ala2776=
XM_017013112.1:c.6999T>C	XP_016868601.1:p.Ala2333=
XM_024447074.1:c.10227T>C	XP_024302842.1:p.Ala3409=
NM_017890.5:c.11442T>C MANE Plus Clinical	NP_060360.3:p.Ala3814=
NM_152564.5:c.11367T>C MANE Select	NP_689777.3:p.Ala3789=