Canonical Allele Identifier: CA2805218304

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022483_91022484insA , CM000677.2:g.91022483_91022484insA	GRCh38
NC_000015.9:g.91565713_91565714insA , CM000677.1:g.91565713_91565714insA	GRCh37
NC_000015.8:g.89366717_89366718insA	NCBI36
NG_012162.1:g.5120_5121insT , LRG_884:g.5120_5121insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-235_-234insT MANE Select	ENSP00000327650.4:n.-235_-234insT
ENST00000643536.1:c.-235_-234insT	ENSP00000494429.1:n.-235_-234insT
ENST00000333371.7:c.-235_-234insT	ENSP00000327650.3:n.-235_-234insT
ENST00000535906.1:c.-235_-234insT	ENSP00000444053.1:n.-235_-234insT
ENST00000556096.6:n.120_121insT
ENST00000557358.1:n.113_114insT
ENST00000574755.5:c.-235_-234insT	ENSP00000460413.1:n.-235_-234insT
NM_001289148.1:c.-235_-234insT	NP_001276077.1:n.-235_-234insT
NM_001289149.1:c.-446_-445insT	NP_001276078.1:n.-446_-445insT
NM_018668.4:c.-235_-234insT , LRG_884t1:c.-235_-234insT	NP_061138.3:n.-235_-234insT
XM_005254884.2:c.-235_-234insT	XP_005254941.1:n.-235_-234insT
XM_005254887.1:c.-365_-364insT	XP_005254944.1:n.-365_-364insT
XM_005254888.2:c.-235_-234insT	XP_005254945.1:n.-235_-234insT
XM_011521448.1:c.-548_-547insT	XP_011519750.1:n.-548_-547insT
XM_017022075.2:c.-596_-595insT	XP_016877564.1:n.-596_-595insT
XM_017022076.1:c.-453_-452insT	XP_016877565.1:n.-453_-452insT
XR_001751213.2:n.102_103insT
NM_018668.5:c.-235_-234insT MANE Select	NP_061138.3:n.-235_-234insT