Canonical Allele Identifier: CA2781481467

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868592_99868593insAGT , CM000670.2:g.99868592_99868593insAGT	GRCh38
NC_000008.10:g.100880820_100880821insAGT , CM000670.1:g.100880820_100880821insAGT	GRCh37
NC_000008.9:g.100949996_100949997insAGT	NCBI36
NG_007098.2:g.860327_860328insAGT , LRG_351:g.860327_860328insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*561+127_*561+128insAGT	ENSP00000507923.1:n.*561+127_*561+128insAGT
ENST00000682358.1:n.11537+127_11537+128insAGT
ENST00000683334.1:c.*7149+127_*7149+128insAGT	ENSP00000507369.1:n.*7149+127_*7149+128insAGT
ENST00000357162.7:c.11392+127_11392+128insAGT MANE Select	ENSP00000349685.2:n.11392+127_11392+128insAGT
ENST00000358544.7:c.11467+127_11467+128insAGT MANE Plus Clinical	ENSP00000351346.2:n.11467+127_11467+128insAGT
ENST00000357162.6:c.11392+127_11392+128insAGT	ENSP00000349685.2:n.11392+127_11392+128insAGT
ENST00000358544.6:c.11467+127_11467+128insAGT	ENSP00000351346.2:n.11467+127_11467+128insAGT
ENST00000493587.1:n.409+127_409+128insAGT
NM_017890.4:c.11467+127_11467+128insAGT , LRG_351t1:c.11467+127_11467+128insAGT	NP_060360.3:n.11467+127_11467+128insAGT
NM_152564.4:c.11392+127_11392+128insAGT , LRG_351t2:c.11392+127_11392+128insAGT	NP_689777.3:n.11392+127_11392+128insAGT
XM_005250800.2:c.11467+127_11467+128insAGT	XP_005250857.1:n.11467+127_11467+128insAGT
XM_005250801.3:c.11467+127_11467+128insAGT	XP_005250858.1:n.11467+127_11467+128insAGT
XM_011516848.1:c.11464+127_11464+128insAGT	XP_011515150.1:n.11464+127_11464+128insAGT
XM_011516849.1:c.11389+127_11389+128insAGT	XP_011515151.1:n.11389+127_11389+128insAGT
XM_011516850.1:c.11089+127_11089+128insAGT	XP_011515152.1:n.11089+127_11089+128insAGT
XM_011516851.1:c.8353+127_8353+128insAGT	XP_011515153.1:n.8353+127_8353+128insAGT
XM_011516852.1:c.8353+127_8353+128insAGT	XP_011515154.1:n.8353+127_8353+128insAGT
XM_011516854.1:c.7246+127_7246+128insAGT	XP_011515156.1:n.7246+127_7246+128insAGT
XM_005250800.3:c.11467+127_11467+128insAGT	XP_005250857.1:n.11467+127_11467+128insAGT
XM_005250801.5:c.11467+127_11467+128insAGT	XP_005250858.1:n.11467+127_11467+128insAGT
XM_011516848.2:c.11464+127_11464+128insAGT	XP_011515150.1:n.11464+127_11464+128insAGT
XM_011516849.2:c.11389+127_11389+128insAGT	XP_011515151.1:n.11389+127_11389+128insAGT
XM_011516850.2:c.11089+127_11089+128insAGT	XP_011515152.1:n.11089+127_11089+128insAGT
XM_011516851.2:c.8353+127_8353+128insAGT	XP_011515153.1:n.8353+127_8353+128insAGT
XM_011516852.2:c.8353+127_8353+128insAGT	XP_011515154.1:n.8353+127_8353+128insAGT
XM_011516854.2:c.7246+127_7246+128insAGT	XP_011515156.1:n.7246+127_7246+128insAGT
XM_017013109.1:c.11272+127_11272+128insAGT	XP_016868598.1:n.11272+127_11272+128insAGT
XM_017013111.1:c.8353+127_8353+128insAGT	XP_016868600.1:n.8353+127_8353+128insAGT
XM_017013112.1:c.7024+127_7024+128insAGT	XP_016868601.1:n.7024+127_7024+128insAGT
XM_024447074.1:c.10252+127_10252+128insAGT	XP_024302842.1:n.10252+127_10252+128insAGT
NM_017890.5:c.11467+127_11467+128insAGT MANE Plus Clinical	NP_060360.3:n.11467+127_11467+128insAGT
NM_152564.5:c.11392+127_11392+128insAGT MANE Select	NP_689777.3:n.11392+127_11392+128insAGT