Canonical Allele Identifier: CA2781481417

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868530_99868531insAG , CM000670.2:g.99868530_99868531insAG	GRCh38
NC_000008.10:g.100880758_100880759insAG , CM000670.1:g.100880758_100880759insAG	GRCh37
NC_000008.9:g.100949934_100949935insAG	NCBI36
NG_007098.2:g.860265_860266insAG , LRG_351:g.860265_860266insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*561+65_*561+66insAG	ENSP00000507923.1:n.*561+65_*561+66insAG
ENST00000682358.1:n.11537+65_11537+66insAG
ENST00000683334.1:c.*7149+65_*7149+66insAG	ENSP00000507369.1:n.*7149+65_*7149+66insAG
ENST00000357162.7:c.11392+65_11392+66insAG MANE Select	ENSP00000349685.2:n.11392+65_11392+66insAG
ENST00000358544.7:c.11467+65_11467+66insAG MANE Plus Clinical	ENSP00000351346.2:n.11467+65_11467+66insAG
ENST00000357162.6:c.11392+65_11392+66insAG	ENSP00000349685.2:n.11392+65_11392+66insAG
ENST00000358544.6:c.11467+65_11467+66insAG	ENSP00000351346.2:n.11467+65_11467+66insAG
ENST00000493587.1:n.409+65_409+66insAG
NM_017890.4:c.11467+65_11467+66insAG , LRG_351t1:c.11467+65_11467+66insAG	NP_060360.3:n.11467+65_11467+66insAG
NM_152564.4:c.11392+65_11392+66insAG , LRG_351t2:c.11392+65_11392+66insAG	NP_689777.3:n.11392+65_11392+66insAG
XM_005250800.2:c.11467+65_11467+66insAG	XP_005250857.1:n.11467+65_11467+66insAG
XM_005250801.3:c.11467+65_11467+66insAG	XP_005250858.1:n.11467+65_11467+66insAG
XM_011516848.1:c.11464+65_11464+66insAG	XP_011515150.1:n.11464+65_11464+66insAG
XM_011516849.1:c.11389+65_11389+66insAG	XP_011515151.1:n.11389+65_11389+66insAG
XM_011516850.1:c.11089+65_11089+66insAG	XP_011515152.1:n.11089+65_11089+66insAG
XM_011516851.1:c.8353+65_8353+66insAG	XP_011515153.1:n.8353+65_8353+66insAG
XM_011516852.1:c.8353+65_8353+66insAG	XP_011515154.1:n.8353+65_8353+66insAG
XM_011516854.1:c.7246+65_7246+66insAG	XP_011515156.1:n.7246+65_7246+66insAG
XM_005250800.3:c.11467+65_11467+66insAG	XP_005250857.1:n.11467+65_11467+66insAG
XM_005250801.5:c.11467+65_11467+66insAG	XP_005250858.1:n.11467+65_11467+66insAG
XM_011516848.2:c.11464+65_11464+66insAG	XP_011515150.1:n.11464+65_11464+66insAG
XM_011516849.2:c.11389+65_11389+66insAG	XP_011515151.1:n.11389+65_11389+66insAG
XM_011516850.2:c.11089+65_11089+66insAG	XP_011515152.1:n.11089+65_11089+66insAG
XM_011516851.2:c.8353+65_8353+66insAG	XP_011515153.1:n.8353+65_8353+66insAG
XM_011516852.2:c.8353+65_8353+66insAG	XP_011515154.1:n.8353+65_8353+66insAG
XM_011516854.2:c.7246+65_7246+66insAG	XP_011515156.1:n.7246+65_7246+66insAG
XM_017013109.1:c.11272+65_11272+66insAG	XP_016868598.1:n.11272+65_11272+66insAG
XM_017013111.1:c.8353+65_8353+66insAG	XP_016868600.1:n.8353+65_8353+66insAG
XM_017013112.1:c.7024+65_7024+66insAG	XP_016868601.1:n.7024+65_7024+66insAG
XM_024447074.1:c.10252+65_10252+66insAG	XP_024302842.1:n.10252+65_10252+66insAG
NM_017890.5:c.11467+65_11467+66insAG MANE Plus Clinical	NP_060360.3:n.11467+65_11467+66insAG
NM_152564.5:c.11392+65_11392+66insAG MANE Select	NP_689777.3:n.11392+65_11392+66insAG