Canonical Allele Identifier: CA462448930

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100779046T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99766818T>C , CM000670.2:g.99766818T>C	GRCh38
NC_000008.10:g.100779046T>C , CM000670.1:g.100779046T>C	GRCh37
NC_000008.9:g.100848222T>C	NCBI36
NG_007098.2:g.758553T>C , LRG_351:g.758553T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.7170T>C	ENSP00000507923.1:p.Phe2390=
ENST00000682358.1:n.7240T>C
ENST00000683334.1:c.*2852T>C	ENSP00000507369.1:n.*2852T>C
ENST00000357162.7:c.7095T>C MANE Select	ENSP00000349685.2:p.Phe2365=
ENST00000358544.7:c.7170T>C MANE Plus Clinical	ENSP00000351346.2:p.Phe2390=
ENST00000357162.6:c.7095T>C	ENSP00000349685.2:p.Phe2365=
ENST00000358544.6:c.7170T>C	ENSP00000351346.2:p.Phe2390=
ENST00000518569.1:n.225T>C
NM_017890.4:c.7170T>C , LRG_351t1:c.7170T>C	NP_060360.3:p.Phe2390=
NM_152564.4:c.7095T>C , LRG_351t2:c.7095T>C	NP_689777.3:p.Phe2365=
XM_005250800.2:c.7170T>C	XP_005250857.1:p.Phe2390=
XM_005250801.3:c.7170T>C	XP_005250858.1:p.Phe2390=
XM_011516848.1:c.7167T>C	XP_011515150.1:p.Phe2389=
XM_011516849.1:c.7092T>C	XP_011515151.1:p.Phe2364=
XM_011516850.1:c.6792T>C	XP_011515152.1:p.Phe2264=
XM_011516851.1:c.4056T>C	XP_011515153.1:p.Phe1352=
XM_011516852.1:c.4056T>C	XP_011515154.1:p.Phe1352=
XM_011516853.1:c.7170T>C	XP_011515155.1:p.Phe2390=
XM_011516854.1:c.2949T>C	XP_011515156.1:p.Phe983=
XR_928446.1:n.2065+3870A>G
XM_005250800.3:c.7170T>C	XP_005250857.1:p.Phe2390=
XM_005250801.5:c.7170T>C	XP_005250858.1:p.Phe2390=
XM_011516848.2:c.7167T>C	XP_011515150.1:p.Phe2389=
XM_011516849.2:c.7092T>C	XP_011515151.1:p.Phe2364=
XM_011516850.2:c.6792T>C	XP_011515152.1:p.Phe2264=
XM_011516851.2:c.4056T>C	XP_011515153.1:p.Phe1352=
XM_011516852.2:c.4056T>C	XP_011515154.1:p.Phe1352=
XM_011516853.2:c.7170T>C	XP_011515155.1:p.Phe2390=
XM_011516854.2:c.2949T>C	XP_011515156.1:p.Phe983=
XM_017013109.1:c.6975T>C	XP_016868598.1:p.Phe2325=
XM_017013111.1:c.4056T>C	XP_016868600.1:p.Phe1352=
XM_017013112.1:c.2727T>C	XP_016868601.1:p.Phe909=
XM_024447074.1:c.5955T>C	XP_024302842.1:p.Phe1985=
NM_017890.5:c.7170T>C MANE Plus Clinical	NP_060360.3:p.Phe2390=
NM_152564.5:c.7095T>C MANE Select	NP_689777.3:p.Phe2365=