Canonical Allele Identifier: CA2781478422

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99777012_99777013insAG , CM000670.2:g.99777012_99777013insAG	GRCh38
NC_000008.10:g.100789240_100789241insAG , CM000670.1:g.100789240_100789241insAG	GRCh37
NC_000008.9:g.100858416_100858417insAG	NCBI36
NG_007098.2:g.768747_768748insAG , LRG_351:g.768747_768748insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.7504+56_7504+57insAG	ENSP00000507923.1:n.7504+56_7504+57insAG
ENST00000682358.1:n.7574+56_7574+57insAG
ENST00000683334.1:c.*3186+56_*3186+57insAG	ENSP00000507369.1:n.*3186+56_*3186+57insAG
ENST00000357162.7:c.7429+56_7429+57insAG MANE Select	ENSP00000349685.2:n.7429+56_7429+57insAG
ENST00000358544.7:c.7504+56_7504+57insAG MANE Plus Clinical	ENSP00000351346.2:n.7504+56_7504+57insAG
ENST00000357162.6:c.7429+56_7429+57insAG	ENSP00000349685.2:n.7429+56_7429+57insAG
ENST00000358544.6:c.7504+56_7504+57insAG	ENSP00000351346.2:n.7504+56_7504+57insAG
ENST00000518569.1:n.378-1670_378-1669insAG
NM_017890.4:c.7504+56_7504+57insAG , LRG_351t1:c.7504+56_7504+57insAG	NP_060360.3:n.7504+56_7504+57insAG
NM_152564.4:c.7429+56_7429+57insAG , LRG_351t2:c.7429+56_7429+57insAG	NP_689777.3:n.7429+56_7429+57insAG
XM_005250800.2:c.7504+56_7504+57insAG	XP_005250857.1:n.7504+56_7504+57insAG
XM_005250801.3:c.7504+56_7504+57insAG	XP_005250858.1:n.7504+56_7504+57insAG
XM_011516848.1:c.7501+56_7501+57insAG	XP_011515150.1:n.7501+56_7501+57insAG
XM_011516849.1:c.7426+56_7426+57insAG	XP_011515151.1:n.7426+56_7426+57insAG
XM_011516850.1:c.7126+56_7126+57insAG	XP_011515152.1:n.7126+56_7126+57insAG
XM_011516851.1:c.4390+56_4390+57insAG	XP_011515153.1:n.4390+56_4390+57insAG
XM_011516852.1:c.4390+56_4390+57insAG	XP_011515154.1:n.4390+56_4390+57insAG
XM_011516853.1:c.7504+56_7504+57insAG	XP_011515155.1:n.7504+56_7504+57insAG
XM_011516854.1:c.3283+56_3283+57insAG	XP_011515156.1:n.3283+56_3283+57insAG
XR_928446.1:n.1830+5465_1830+5466insCT
XM_005250800.3:c.7504+56_7504+57insAG	XP_005250857.1:n.7504+56_7504+57insAG
XM_005250801.5:c.7504+56_7504+57insAG	XP_005250858.1:n.7504+56_7504+57insAG
XM_011516848.2:c.7501+56_7501+57insAG	XP_011515150.1:n.7501+56_7501+57insAG
XM_011516849.2:c.7426+56_7426+57insAG	XP_011515151.1:n.7426+56_7426+57insAG
XM_011516850.2:c.7126+56_7126+57insAG	XP_011515152.1:n.7126+56_7126+57insAG
XM_011516851.2:c.4390+56_4390+57insAG	XP_011515153.1:n.4390+56_4390+57insAG
XM_011516852.2:c.4390+56_4390+57insAG	XP_011515154.1:n.4390+56_4390+57insAG
XM_011516853.2:c.7504+56_7504+57insAG	XP_011515155.1:n.7504+56_7504+57insAG
XM_011516854.2:c.3283+56_3283+57insAG	XP_011515156.1:n.3283+56_3283+57insAG
XM_017013109.1:c.7309+56_7309+57insAG	XP_016868598.1:n.7309+56_7309+57insAG
XM_017013111.1:c.4390+56_4390+57insAG	XP_016868600.1:n.4390+56_4390+57insAG
XM_017013112.1:c.3061+56_3061+57insAG	XP_016868601.1:n.3061+56_3061+57insAG
XM_024447074.1:c.6289+56_6289+57insAG	XP_024302842.1:n.6289+56_6289+57insAG
NM_017890.5:c.7504+56_7504+57insAG MANE Plus Clinical	NP_060360.3:n.7504+56_7504+57insAG
NM_152564.5:c.7429+56_7429+57insAG MANE Select	NP_689777.3:n.7429+56_7429+57insAG