Canonical Allele Identifier: CA2781481473

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868600_99868601insGAT , CM000670.2:g.99868600_99868601insGAT	GRCh38
NC_000008.10:g.100880828_100880829insGAT , CM000670.1:g.100880828_100880829insGAT	GRCh37
NC_000008.9:g.100950004_100950005insGAT	NCBI36
NG_007098.2:g.860335_860336insGAT , LRG_351:g.860335_860336insGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*561+135_*561+136insGAT	ENSP00000507923.1:n.*561+135_*561+136insGAT
ENST00000682358.1:n.11537+135_11537+136insGAT
ENST00000683334.1:c.*7149+135_*7149+136insGAT	ENSP00000507369.1:n.*7149+135_*7149+136insGAT
ENST00000357162.7:c.11392+135_11392+136insGAT MANE Select	ENSP00000349685.2:n.11392+135_11392+136insGAT
ENST00000358544.7:c.11467+135_11467+136insGAT MANE Plus Clinical	ENSP00000351346.2:n.11467+135_11467+136insGAT
ENST00000357162.6:c.11392+135_11392+136insGAT	ENSP00000349685.2:n.11392+135_11392+136insGAT
ENST00000358544.6:c.11467+135_11467+136insGAT	ENSP00000351346.2:n.11467+135_11467+136insGAT
ENST00000493587.1:n.409+135_409+136insGAT
NM_017890.4:c.11467+135_11467+136insGAT , LRG_351t1:c.11467+135_11467+136insGAT	NP_060360.3:n.11467+135_11467+136insGAT
NM_152564.4:c.11392+135_11392+136insGAT , LRG_351t2:c.11392+135_11392+136insGAT	NP_689777.3:n.11392+135_11392+136insGAT
XM_005250800.2:c.11467+135_11467+136insGAT	XP_005250857.1:n.11467+135_11467+136insGAT
XM_005250801.3:c.11467+135_11467+136insGAT	XP_005250858.1:n.11467+135_11467+136insGAT
XM_011516848.1:c.11464+135_11464+136insGAT	XP_011515150.1:n.11464+135_11464+136insGAT
XM_011516849.1:c.11389+135_11389+136insGAT	XP_011515151.1:n.11389+135_11389+136insGAT
XM_011516850.1:c.11089+135_11089+136insGAT	XP_011515152.1:n.11089+135_11089+136insGAT
XM_011516851.1:c.8353+135_8353+136insGAT	XP_011515153.1:n.8353+135_8353+136insGAT
XM_011516852.1:c.8353+135_8353+136insGAT	XP_011515154.1:n.8353+135_8353+136insGAT
XM_011516854.1:c.7246+135_7246+136insGAT	XP_011515156.1:n.7246+135_7246+136insGAT
XM_005250800.3:c.11467+135_11467+136insGAT	XP_005250857.1:n.11467+135_11467+136insGAT
XM_005250801.5:c.11467+135_11467+136insGAT	XP_005250858.1:n.11467+135_11467+136insGAT
XM_011516848.2:c.11464+135_11464+136insGAT	XP_011515150.1:n.11464+135_11464+136insGAT
XM_011516849.2:c.11389+135_11389+136insGAT	XP_011515151.1:n.11389+135_11389+136insGAT
XM_011516850.2:c.11089+135_11089+136insGAT	XP_011515152.1:n.11089+135_11089+136insGAT
XM_011516851.2:c.8353+135_8353+136insGAT	XP_011515153.1:n.8353+135_8353+136insGAT
XM_011516852.2:c.8353+135_8353+136insGAT	XP_011515154.1:n.8353+135_8353+136insGAT
XM_011516854.2:c.7246+135_7246+136insGAT	XP_011515156.1:n.7246+135_7246+136insGAT
XM_017013109.1:c.11272+135_11272+136insGAT	XP_016868598.1:n.11272+135_11272+136insGAT
XM_017013111.1:c.8353+135_8353+136insGAT	XP_016868600.1:n.8353+135_8353+136insGAT
XM_017013112.1:c.7024+135_7024+136insGAT	XP_016868601.1:n.7024+135_7024+136insGAT
XM_024447074.1:c.10252+135_10252+136insGAT	XP_024302842.1:n.10252+135_10252+136insGAT
NM_017890.5:c.11467+135_11467+136insGAT MANE Plus Clinical	NP_060360.3:n.11467+135_11467+136insGAT
NM_152564.5:c.11392+135_11392+136insGAT MANE Select	NP_689777.3:n.11392+135_11392+136insGAT