Canonical Allele Identifier: CA2781481447

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868569_99868570insAC , CM000670.2:g.99868569_99868570insAC	GRCh38
NC_000008.10:g.100880797_100880798insAC , CM000670.1:g.100880797_100880798insAC	GRCh37
NC_000008.9:g.100949973_100949974insAC	NCBI36
NG_007098.2:g.860304_860305insAC , LRG_351:g.860304_860305insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*561+104_*561+105insAC	ENSP00000507923.1:n.*561+104_*561+105insAC
ENST00000682358.1:n.11537+104_11537+105insAC
ENST00000683334.1:c.*7149+104_*7149+105insAC	ENSP00000507369.1:n.*7149+104_*7149+105insAC
ENST00000357162.7:c.11392+104_11392+105insAC MANE Select	ENSP00000349685.2:n.11392+104_11392+105insAC
ENST00000358544.7:c.11467+104_11467+105insAC MANE Plus Clinical	ENSP00000351346.2:n.11467+104_11467+105insAC
ENST00000357162.6:c.11392+104_11392+105insAC	ENSP00000349685.2:n.11392+104_11392+105insAC
ENST00000358544.6:c.11467+104_11467+105insAC	ENSP00000351346.2:n.11467+104_11467+105insAC
ENST00000493587.1:n.409+104_409+105insAC
NM_017890.4:c.11467+104_11467+105insAC , LRG_351t1:c.11467+104_11467+105insAC	NP_060360.3:n.11467+104_11467+105insAC
NM_152564.4:c.11392+104_11392+105insAC , LRG_351t2:c.11392+104_11392+105insAC	NP_689777.3:n.11392+104_11392+105insAC
XM_005250800.2:c.11467+104_11467+105insAC	XP_005250857.1:n.11467+104_11467+105insAC
XM_005250801.3:c.11467+104_11467+105insAC	XP_005250858.1:n.11467+104_11467+105insAC
XM_011516848.1:c.11464+104_11464+105insAC	XP_011515150.1:n.11464+104_11464+105insAC
XM_011516849.1:c.11389+104_11389+105insAC	XP_011515151.1:n.11389+104_11389+105insAC
XM_011516850.1:c.11089+104_11089+105insAC	XP_011515152.1:n.11089+104_11089+105insAC
XM_011516851.1:c.8353+104_8353+105insAC	XP_011515153.1:n.8353+104_8353+105insAC
XM_011516852.1:c.8353+104_8353+105insAC	XP_011515154.1:n.8353+104_8353+105insAC
XM_011516854.1:c.7246+104_7246+105insAC	XP_011515156.1:n.7246+104_7246+105insAC
XM_005250800.3:c.11467+104_11467+105insAC	XP_005250857.1:n.11467+104_11467+105insAC
XM_005250801.5:c.11467+104_11467+105insAC	XP_005250858.1:n.11467+104_11467+105insAC
XM_011516848.2:c.11464+104_11464+105insAC	XP_011515150.1:n.11464+104_11464+105insAC
XM_011516849.2:c.11389+104_11389+105insAC	XP_011515151.1:n.11389+104_11389+105insAC
XM_011516850.2:c.11089+104_11089+105insAC	XP_011515152.1:n.11089+104_11089+105insAC
XM_011516851.2:c.8353+104_8353+105insAC	XP_011515153.1:n.8353+104_8353+105insAC
XM_011516852.2:c.8353+104_8353+105insAC	XP_011515154.1:n.8353+104_8353+105insAC
XM_011516854.2:c.7246+104_7246+105insAC	XP_011515156.1:n.7246+104_7246+105insAC
XM_017013109.1:c.11272+104_11272+105insAC	XP_016868598.1:n.11272+104_11272+105insAC
XM_017013111.1:c.8353+104_8353+105insAC	XP_016868600.1:n.8353+104_8353+105insAC
XM_017013112.1:c.7024+104_7024+105insAC	XP_016868601.1:n.7024+104_7024+105insAC
XM_024447074.1:c.10252+104_10252+105insAC	XP_024302842.1:n.10252+104_10252+105insAC
NM_017890.5:c.11467+104_11467+105insAC MANE Plus Clinical	NP_060360.3:n.11467+104_11467+105insAC
NM_152564.5:c.11392+104_11392+105insAC MANE Select	NP_689777.3:n.11392+104_11392+105insAC