Canonical Allele Identifier: CA2781481469

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868593_99868599del , CM000670.2:g.99868593_99868599del	GRCh38
NC_000008.10:g.100880821_100880827del , CM000670.1:g.100880821_100880827del	GRCh37
NC_000008.9:g.100949997_100950003del	NCBI36
NG_007098.2:g.860328_860334del , LRG_351:g.860328_860334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*561+128_*561+134del	ENSP00000507923.1:n.*561+128_*561+134del
ENST00000682358.1:n.11537+128_11537+134del
ENST00000683334.1:c.*7149+128_*7149+134del	ENSP00000507369.1:n.*7149+128_*7149+134del
ENST00000357162.7:c.11392+128_11392+134del MANE Select	ENSP00000349685.2:n.11392+128_11392+134del
ENST00000358544.7:c.11467+128_11467+134del MANE Plus Clinical	ENSP00000351346.2:n.11467+128_11467+134del
ENST00000357162.6:c.11392+128_11392+134del	ENSP00000349685.2:n.11392+128_11392+134del
ENST00000358544.6:c.11467+128_11467+134del	ENSP00000351346.2:n.11467+128_11467+134del
ENST00000493587.1:n.409+128_409+134del
NM_017890.4:c.11467+128_11467+134del , LRG_351t1:c.11467+128_11467+134del	NP_060360.3:n.11467+128_11467+134del
NM_152564.4:c.11392+128_11392+134del , LRG_351t2:c.11392+128_11392+134del	NP_689777.3:n.11392+128_11392+134del
XM_005250800.2:c.11467+128_11467+134del	XP_005250857.1:n.11467+128_11467+134del
XM_005250801.3:c.11467+128_11467+134del	XP_005250858.1:n.11467+128_11467+134del
XM_011516848.1:c.11464+128_11464+134del	XP_011515150.1:n.11464+128_11464+134del
XM_011516849.1:c.11389+128_11389+134del	XP_011515151.1:n.11389+128_11389+134del
XM_011516850.1:c.11089+128_11089+134del	XP_011515152.1:n.11089+128_11089+134del
XM_011516851.1:c.8353+128_8353+134del	XP_011515153.1:n.8353+128_8353+134del
XM_011516852.1:c.8353+128_8353+134del	XP_011515154.1:n.8353+128_8353+134del
XM_011516854.1:c.7246+128_7246+134del	XP_011515156.1:n.7246+128_7246+134del
XM_005250800.3:c.11467+128_11467+134del	XP_005250857.1:n.11467+128_11467+134del
XM_005250801.5:c.11467+128_11467+134del	XP_005250858.1:n.11467+128_11467+134del
XM_011516848.2:c.11464+128_11464+134del	XP_011515150.1:n.11464+128_11464+134del
XM_011516849.2:c.11389+128_11389+134del	XP_011515151.1:n.11389+128_11389+134del
XM_011516850.2:c.11089+128_11089+134del	XP_011515152.1:n.11089+128_11089+134del
XM_011516851.2:c.8353+128_8353+134del	XP_011515153.1:n.8353+128_8353+134del
XM_011516852.2:c.8353+128_8353+134del	XP_011515154.1:n.8353+128_8353+134del
XM_011516854.2:c.7246+128_7246+134del	XP_011515156.1:n.7246+128_7246+134del
XM_017013109.1:c.11272+128_11272+134del	XP_016868598.1:n.11272+128_11272+134del
XM_017013111.1:c.8353+128_8353+134del	XP_016868600.1:n.8353+128_8353+134del
XM_017013112.1:c.7024+128_7024+134del	XP_016868601.1:n.7024+128_7024+134del
XM_024447074.1:c.10252+128_10252+134del	XP_024302842.1:n.10252+128_10252+134del
NM_017890.5:c.11467+128_11467+134del MANE Plus Clinical	NP_060360.3:n.11467+128_11467+134del
NM_152564.5:c.11392+128_11392+134del MANE Select	NP_689777.3:n.11392+128_11392+134del