Canonical Allele Identifier: CA2781478475

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99777055_99777062del , CM000670.2:g.99777055_99777062del	GRCh38
NC_000008.10:g.100789283_100789290del , CM000670.1:g.100789283_100789290del	GRCh37
NC_000008.9:g.100858459_100858466del	NCBI36
NG_007098.2:g.768790_768797del , LRG_351:g.768790_768797del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7504+99_7504+106del	ENSP00000507923.1:n.7504+99_7504+106del
ENST00000682358.1:n.7574+99_7574+106del
ENST00000683334.1:c.*3186+99_*3186+106del	ENSP00000507369.1:n.*3186+99_*3186+106del
ENST00000357162.7:c.7429+99_7429+106del MANE Select	ENSP00000349685.2:n.7429+99_7429+106del
ENST00000358544.7:c.7504+99_7504+106del MANE Plus Clinical	ENSP00000351346.2:n.7504+99_7504+106del
ENST00000357162.6:c.7429+99_7429+106del	ENSP00000349685.2:n.7429+99_7429+106del
ENST00000358544.6:c.7504+99_7504+106del	ENSP00000351346.2:n.7504+99_7504+106del
ENST00000518569.1:n.378-1627_378-1620del
NM_017890.4:c.7504+99_7504+106del , LRG_351t1:c.7504+99_7504+106del	NP_060360.3:n.7504+99_7504+106del
NM_152564.4:c.7429+99_7429+106del , LRG_351t2:c.7429+99_7429+106del	NP_689777.3:n.7429+99_7429+106del
XM_005250800.2:c.7504+99_7504+106del	XP_005250857.1:n.7504+99_7504+106del
XM_005250801.3:c.7504+99_7504+106del	XP_005250858.1:n.7504+99_7504+106del
XM_011516848.1:c.7501+99_7501+106del	XP_011515150.1:n.7501+99_7501+106del
XM_011516849.1:c.7426+99_7426+106del	XP_011515151.1:n.7426+99_7426+106del
XM_011516850.1:c.7126+99_7126+106del	XP_011515152.1:n.7126+99_7126+106del
XM_011516851.1:c.4390+99_4390+106del	XP_011515153.1:n.4390+99_4390+106del
XM_011516852.1:c.4390+99_4390+106del	XP_011515154.1:n.4390+99_4390+106del
XM_011516853.1:c.7504+99_7504+106del	XP_011515155.1:n.7504+99_7504+106del
XM_011516854.1:c.3283+99_3283+106del	XP_011515156.1:n.3283+99_3283+106del
XR_928446.1:n.1830+5416_1830+5423del
XM_005250800.3:c.7504+99_7504+106del	XP_005250857.1:n.7504+99_7504+106del
XM_005250801.5:c.7504+99_7504+106del	XP_005250858.1:n.7504+99_7504+106del
XM_011516848.2:c.7501+99_7501+106del	XP_011515150.1:n.7501+99_7501+106del
XM_011516849.2:c.7426+99_7426+106del	XP_011515151.1:n.7426+99_7426+106del
XM_011516850.2:c.7126+99_7126+106del	XP_011515152.1:n.7126+99_7126+106del
XM_011516851.2:c.4390+99_4390+106del	XP_011515153.1:n.4390+99_4390+106del
XM_011516852.2:c.4390+99_4390+106del	XP_011515154.1:n.4390+99_4390+106del
XM_011516853.2:c.7504+99_7504+106del	XP_011515155.1:n.7504+99_7504+106del
XM_011516854.2:c.3283+99_3283+106del	XP_011515156.1:n.3283+99_3283+106del
XM_017013109.1:c.7309+99_7309+106del	XP_016868598.1:n.7309+99_7309+106del
XM_017013111.1:c.4390+99_4390+106del	XP_016868600.1:n.4390+99_4390+106del
XM_017013112.1:c.3061+99_3061+106del	XP_016868601.1:n.3061+99_3061+106del
XM_024447074.1:c.6289+99_6289+106del	XP_024302842.1:n.6289+99_6289+106del
NM_017890.5:c.7504+99_7504+106del MANE Plus Clinical	NP_060360.3:n.7504+99_7504+106del
NM_152564.5:c.7429+99_7429+106del MANE Select	NP_689777.3:n.7429+99_7429+106del