Canonical Allele Identifier: CA2781481432

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868545_99868546insA , CM000670.2:g.99868545_99868546insA	GRCh38
NC_000008.10:g.100880773_100880774insA , CM000670.1:g.100880773_100880774insA	GRCh37
NC_000008.9:g.100949949_100949950insA	NCBI36
NG_007098.2:g.860280_860281insA , LRG_351:g.860280_860281insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*561+80_*561+81insA	ENSP00000507923.1:n.*561+80_*561+81insA
ENST00000682358.1:n.11537+80_11537+81insA
ENST00000683334.1:c.*7149+80_*7149+81insA	ENSP00000507369.1:n.*7149+80_*7149+81insA
ENST00000357162.7:c.11392+80_11392+81insA MANE Select	ENSP00000349685.2:n.11392+80_11392+81insA
ENST00000358544.7:c.11467+80_11467+81insA MANE Plus Clinical	ENSP00000351346.2:n.11467+80_11467+81insA
ENST00000357162.6:c.11392+80_11392+81insA	ENSP00000349685.2:n.11392+80_11392+81insA
ENST00000358544.6:c.11467+80_11467+81insA	ENSP00000351346.2:n.11467+80_11467+81insA
ENST00000493587.1:n.409+80_409+81insA
NM_017890.4:c.11467+80_11467+81insA , LRG_351t1:c.11467+80_11467+81insA	NP_060360.3:n.11467+80_11467+81insA
NM_152564.4:c.11392+80_11392+81insA , LRG_351t2:c.11392+80_11392+81insA	NP_689777.3:n.11392+80_11392+81insA
XM_005250800.2:c.11467+80_11467+81insA	XP_005250857.1:n.11467+80_11467+81insA
XM_005250801.3:c.11467+80_11467+81insA	XP_005250858.1:n.11467+80_11467+81insA
XM_011516848.1:c.11464+80_11464+81insA	XP_011515150.1:n.11464+80_11464+81insA
XM_011516849.1:c.11389+80_11389+81insA	XP_011515151.1:n.11389+80_11389+81insA
XM_011516850.1:c.11089+80_11089+81insA	XP_011515152.1:n.11089+80_11089+81insA
XM_011516851.1:c.8353+80_8353+81insA	XP_011515153.1:n.8353+80_8353+81insA
XM_011516852.1:c.8353+80_8353+81insA	XP_011515154.1:n.8353+80_8353+81insA
XM_011516854.1:c.7246+80_7246+81insA	XP_011515156.1:n.7246+80_7246+81insA
XM_005250800.3:c.11467+80_11467+81insA	XP_005250857.1:n.11467+80_11467+81insA
XM_005250801.5:c.11467+80_11467+81insA	XP_005250858.1:n.11467+80_11467+81insA
XM_011516848.2:c.11464+80_11464+81insA	XP_011515150.1:n.11464+80_11464+81insA
XM_011516849.2:c.11389+80_11389+81insA	XP_011515151.1:n.11389+80_11389+81insA
XM_011516850.2:c.11089+80_11089+81insA	XP_011515152.1:n.11089+80_11089+81insA
XM_011516851.2:c.8353+80_8353+81insA	XP_011515153.1:n.8353+80_8353+81insA
XM_011516852.2:c.8353+80_8353+81insA	XP_011515154.1:n.8353+80_8353+81insA
XM_011516854.2:c.7246+80_7246+81insA	XP_011515156.1:n.7246+80_7246+81insA
XM_017013109.1:c.11272+80_11272+81insA	XP_016868598.1:n.11272+80_11272+81insA
XM_017013111.1:c.8353+80_8353+81insA	XP_016868600.1:n.8353+80_8353+81insA
XM_017013112.1:c.7024+80_7024+81insA	XP_016868601.1:n.7024+80_7024+81insA
XM_024447074.1:c.10252+80_10252+81insA	XP_024302842.1:n.10252+80_10252+81insA
NM_017890.5:c.11467+80_11467+81insA MANE Plus Clinical	NP_060360.3:n.11467+80_11467+81insA
NM_152564.5:c.11392+80_11392+81insA MANE Select	NP_689777.3:n.11392+80_11392+81insA