Canonical Allele Identifier: CA2781478489

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99777064_99777065insACTT , CM000670.2:g.99777064_99777065insACTT	GRCh38
NC_000008.10:g.100789292_100789293insACTT , CM000670.1:g.100789292_100789293insACTT	GRCh37
NC_000008.9:g.100858468_100858469insACTT	NCBI36
NG_007098.2:g.768799_768800insACTT , LRG_351:g.768799_768800insACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7504+108_7504+109insACTT	ENSP00000507923.1:n.7504+108_7504+109insACTT
ENST00000682358.1:n.7574+108_7574+109insACTT
ENST00000683334.1:c.*3186+108_*3186+109insACTT	ENSP00000507369.1:n.*3186+108_*3186+109insACTT
ENST00000357162.7:c.7429+108_7429+109insACTT MANE Select	ENSP00000349685.2:n.7429+108_7429+109insACTT
ENST00000358544.7:c.7504+108_7504+109insACTT MANE Plus Clinical	ENSP00000351346.2:n.7504+108_7504+109insACTT
ENST00000357162.6:c.7429+108_7429+109insACTT	ENSP00000349685.2:n.7429+108_7429+109insACTT
ENST00000358544.6:c.7504+108_7504+109insACTT	ENSP00000351346.2:n.7504+108_7504+109insACTT
ENST00000518569.1:n.378-1618_378-1617insACTT
NM_017890.4:c.7504+108_7504+109insACTT , LRG_351t1:c.7504+108_7504+109insACTT	NP_060360.3:n.7504+108_7504+109insACTT
NM_152564.4:c.7429+108_7429+109insACTT , LRG_351t2:c.7429+108_7429+109insACTT	NP_689777.3:n.7429+108_7429+109insACTT
XM_005250800.2:c.7504+108_7504+109insACTT	XP_005250857.1:n.7504+108_7504+109insACTT
XM_005250801.3:c.7504+108_7504+109insACTT	XP_005250858.1:n.7504+108_7504+109insACTT
XM_011516848.1:c.7501+108_7501+109insACTT	XP_011515150.1:n.7501+108_7501+109insACTT
XM_011516849.1:c.7426+108_7426+109insACTT	XP_011515151.1:n.7426+108_7426+109insACTT
XM_011516850.1:c.7126+108_7126+109insACTT	XP_011515152.1:n.7126+108_7126+109insACTT
XM_011516851.1:c.4390+108_4390+109insACTT	XP_011515153.1:n.4390+108_4390+109insACTT
XM_011516852.1:c.4390+108_4390+109insACTT	XP_011515154.1:n.4390+108_4390+109insACTT
XM_011516853.1:c.7504+108_7504+109insACTT	XP_011515155.1:n.7504+108_7504+109insACTT
XM_011516854.1:c.3283+108_3283+109insACTT	XP_011515156.1:n.3283+108_3283+109insACTT
XR_928446.1:n.1830+5413_1830+5414insAAGT
XM_005250800.3:c.7504+108_7504+109insACTT	XP_005250857.1:n.7504+108_7504+109insACTT
XM_005250801.5:c.7504+108_7504+109insACTT	XP_005250858.1:n.7504+108_7504+109insACTT
XM_011516848.2:c.7501+108_7501+109insACTT	XP_011515150.1:n.7501+108_7501+109insACTT
XM_011516849.2:c.7426+108_7426+109insACTT	XP_011515151.1:n.7426+108_7426+109insACTT
XM_011516850.2:c.7126+108_7126+109insACTT	XP_011515152.1:n.7126+108_7126+109insACTT
XM_011516851.2:c.4390+108_4390+109insACTT	XP_011515153.1:n.4390+108_4390+109insACTT
XM_011516852.2:c.4390+108_4390+109insACTT	XP_011515154.1:n.4390+108_4390+109insACTT
XM_011516853.2:c.7504+108_7504+109insACTT	XP_011515155.1:n.7504+108_7504+109insACTT
XM_011516854.2:c.3283+108_3283+109insACTT	XP_011515156.1:n.3283+108_3283+109insACTT
XM_017013109.1:c.7309+108_7309+109insACTT	XP_016868598.1:n.7309+108_7309+109insACTT
XM_017013111.1:c.4390+108_4390+109insACTT	XP_016868600.1:n.4390+108_4390+109insACTT
XM_017013112.1:c.3061+108_3061+109insACTT	XP_016868601.1:n.3061+108_3061+109insACTT
XM_024447074.1:c.6289+108_6289+109insACTT	XP_024302842.1:n.6289+108_6289+109insACTT
NM_017890.5:c.7504+108_7504+109insACTT MANE Plus Clinical	NP_060360.3:n.7504+108_7504+109insACTT
NM_152564.5:c.7429+108_7429+109insACTT MANE Select	NP_689777.3:n.7429+108_7429+109insACTT