Canonical Allele Identifier: CA371776028

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100831645A>T (hg19) ; chr8:g.99819417A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99819417A>T , CM000670.2:g.99819417A>T	GRCh38
NC_000008.10:g.100831645A>T , CM000670.1:g.100831645A>T	GRCh37
NC_000008.9:g.100900821A>T	NCBI36
NG_007098.2:g.811152A>T , LRG_351:g.811152A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8702A>T	ENSP00000507923.1:p.Glu2901Val
ENST00000682358.1:n.8772A>T
ENST00000683334.1:c.*4384A>T	ENSP00000507369.1:n.*4384A>T
ENST00000357162.7:c.8627A>T MANE Select	ENSP00000349685.2:p.Glu2876Val
ENST00000358544.7:c.8702A>T MANE Plus Clinical	ENSP00000351346.2:p.Glu2901Val
ENST00000357162.6:c.8627A>T	ENSP00000349685.2:p.Glu2876Val
ENST00000358544.6:c.8702A>T	ENSP00000351346.2:p.Glu2901Val
NM_017890.4:c.8702A>T , LRG_351t1:c.8702A>T	NP_060360.3:p.Glu2901Val
NM_152564.4:c.8627A>T , LRG_351t2:c.8627A>T	NP_689777.3:p.Glu2876Val
XM_005250800.2:c.8702A>T	XP_005250857.1:p.Glu2901Val
XM_005250801.3:c.8702A>T	XP_005250858.1:p.Glu2901Val
XM_011516848.1:c.8699A>T	XP_011515150.1:p.Glu2900Val
XM_011516849.1:c.8624A>T	XP_011515151.1:p.Glu2875Val
XM_011516850.1:c.8324A>T	XP_011515152.1:p.Glu2775Val
XM_011516851.1:c.5588A>T	XP_011515153.1:p.Glu1863Val
XM_011516852.1:c.5588A>T	XP_011515154.1:p.Glu1863Val
XM_011516854.1:c.4481A>T	XP_011515156.1:p.Glu1494Val
XM_005250800.3:c.8702A>T	XP_005250857.1:p.Glu2901Val
XM_005250801.5:c.8702A>T	XP_005250858.1:p.Glu2901Val
XM_011516848.2:c.8699A>T	XP_011515150.1:p.Glu2900Val
XM_011516849.2:c.8624A>T	XP_011515151.1:p.Glu2875Val
XM_011516850.2:c.8324A>T	XP_011515152.1:p.Glu2775Val
XM_011516851.2:c.5588A>T	XP_011515153.1:p.Glu1863Val
XM_011516852.2:c.5588A>T	XP_011515154.1:p.Glu1863Val
XM_011516854.2:c.4481A>T	XP_011515156.1:p.Glu1494Val
XM_017013109.1:c.8507A>T	XP_016868598.1:p.Glu2836Val
XM_017013111.1:c.5588A>T	XP_016868600.1:p.Glu1863Val
XM_017013112.1:c.4259A>T	XP_016868601.1:p.Glu1420Val
XM_024447074.1:c.7487A>T	XP_024302842.1:p.Glu2496Val
NM_017890.5:c.8702A>T MANE Plus Clinical	NP_060360.3:p.Glu2901Val
NM_152564.5:c.8627A>T MANE Select	NP_689777.3:p.Glu2876Val