Canonical Allele Identifier: CA462464422

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100654266T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99642038T>A , CM000670.2:g.99642038T>A	GRCh38
NC_000008.10:g.100654266T>A , CM000670.1:g.100654266T>A	GRCh37
NC_000008.9:g.100723442T>A	NCBI36
NG_007098.2:g.633773T>A , LRG_351:g.633773T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.5523T>A	ENSP00000507923.1:p.Ile1841=
ENST00000682358.1:n.5593T>A
ENST00000683334.1:c.*1205T>A	ENSP00000507369.1:n.*1205T>A
ENST00000357162.7:c.5448T>A MANE Select	ENSP00000349685.2:p.Ile1816=
ENST00000358544.7:c.5523T>A MANE Plus Clinical	ENSP00000351346.2:p.Ile1841=
ENST00000357162.6:c.5448T>A	ENSP00000349685.2:p.Ile1816=
ENST00000358544.6:c.5523T>A	ENSP00000351346.2:p.Ile1841=
NM_017890.4:c.5523T>A , LRG_351t1:c.5523T>A	NP_060360.3:p.Ile1841=
NM_152564.4:c.5448T>A , LRG_351t2:c.5448T>A	NP_689777.3:p.Ile1816=
XM_005250800.2:c.5523T>A	XP_005250857.1:p.Ile1841=
XM_005250801.3:c.5523T>A	XP_005250858.1:p.Ile1841=
XM_011516848.1:c.5520T>A	XP_011515150.1:p.Ile1840=
XM_011516849.1:c.5445T>A	XP_011515151.1:p.Ile1815=
XM_011516850.1:c.5145T>A	XP_011515152.1:p.Ile1715=
XM_011516851.1:c.2409T>A	XP_011515153.1:p.Ile803=
XM_011516852.1:c.2409T>A	XP_011515154.1:p.Ile803=
XM_011516853.1:c.5523T>A	XP_011515155.1:p.Ile1841=
XM_011516854.1:c.1302T>A	XP_011515156.1:p.Ile434=
XM_005250800.3:c.5523T>A	XP_005250857.1:p.Ile1841=
XM_005250801.5:c.5523T>A	XP_005250858.1:p.Ile1841=
XM_011516848.2:c.5520T>A	XP_011515150.1:p.Ile1840=
XM_011516849.2:c.5445T>A	XP_011515151.1:p.Ile1815=
XM_011516850.2:c.5145T>A	XP_011515152.1:p.Ile1715=
XM_011516851.2:c.2409T>A	XP_011515153.1:p.Ile803=
XM_011516852.2:c.2409T>A	XP_011515154.1:p.Ile803=
XM_011516853.2:c.5523T>A	XP_011515155.1:p.Ile1841=
XM_011516854.2:c.1302T>A	XP_011515156.1:p.Ile434=
XM_017013109.1:c.5328T>A	XP_016868598.1:p.Ile1776=
XM_017013111.1:c.2409T>A	XP_016868600.1:p.Ile803=
XM_017013112.1:c.1080T>A	XP_016868601.1:p.Ile360=
XM_024447074.1:c.4308T>A	XP_024302842.1:p.Ile1436=
XR_001745482.2:n.5484T>A
NM_017890.5:c.5523T>A MANE Plus Clinical	NP_060360.3:p.Ile1841=
NM_152564.5:c.5448T>A MANE Select	NP_689777.3:p.Ile1816=