Canonical Allele Identifier: CA462339302

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100880611C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868383C>T , CM000670.2:g.99868383C>T	GRCh38
NC_000008.10:g.100880611C>T , CM000670.1:g.100880611C>T	GRCh37
NC_000008.9:g.100949787C>T	NCBI36
NG_007098.2:g.860118C>T , LRG_351:g.860118C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*479C>T	ENSP00000507923.1:n.*479C>T
ENST00000682358.1:n.11455C>T
ENST00000683334.1:c.*7067C>T	ENSP00000507369.1:n.*7067C>T
ENST00000357162.7:c.11310C>T MANE Select	ENSP00000349685.2:p.Ile3770=
ENST00000358544.7:c.11385C>T MANE Plus Clinical	ENSP00000351346.2:p.Ile3795=
ENST00000357162.6:c.11310C>T	ENSP00000349685.2:p.Ile3770=
ENST00000358544.6:c.11385C>T	ENSP00000351346.2:p.Ile3795=
ENST00000493587.1:n.327C>T
NM_017890.4:c.11385C>T , LRG_351t1:c.11385C>T	NP_060360.3:p.Ile3795=
NM_152564.4:c.11310C>T , LRG_351t2:c.11310C>T	NP_689777.3:p.Ile3770=
XM_005250800.2:c.11385C>T	XP_005250857.1:p.Ile3795=
XM_005250801.3:c.11385C>T	XP_005250858.1:p.Ile3795=
XM_011516848.1:c.11382C>T	XP_011515150.1:p.Ile3794=
XM_011516849.1:c.11307C>T	XP_011515151.1:p.Ile3769=
XM_011516850.1:c.11007C>T	XP_011515152.1:p.Ile3669=
XM_011516851.1:c.8271C>T	XP_011515153.1:p.Ile2757=
XM_011516852.1:c.8271C>T	XP_011515154.1:p.Ile2757=
XM_011516854.1:c.7164C>T	XP_011515156.1:p.Ile2388=
XM_005250800.3:c.11385C>T	XP_005250857.1:p.Ile3795=
XM_005250801.5:c.11385C>T	XP_005250858.1:p.Ile3795=
XM_011516848.2:c.11382C>T	XP_011515150.1:p.Ile3794=
XM_011516849.2:c.11307C>T	XP_011515151.1:p.Ile3769=
XM_011516850.2:c.11007C>T	XP_011515152.1:p.Ile3669=
XM_011516851.2:c.8271C>T	XP_011515153.1:p.Ile2757=
XM_011516852.2:c.8271C>T	XP_011515154.1:p.Ile2757=
XM_011516854.2:c.7164C>T	XP_011515156.1:p.Ile2388=
XM_017013109.1:c.11190C>T	XP_016868598.1:p.Ile3730=
XM_017013111.1:c.8271C>T	XP_016868600.1:p.Ile2757=
XM_017013112.1:c.6942C>T	XP_016868601.1:p.Ile2314=
XM_024447074.1:c.10170C>T	XP_024302842.1:p.Ile3390=
NM_017890.5:c.11385C>T MANE Plus Clinical	NP_060360.3:p.Ile3795=
NM_152564.5:c.11310C>T MANE Select	NP_689777.3:p.Ile3770=