Canonical Allele Identifier: CA2195408462

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022424_91022425delinsGC , CM000677.2:g.91022424_91022425delinsGC	GRCh38
NC_000015.9:g.91565654_91565655delinsGC , CM000677.1:g.91565654_91565655delinsGC	GRCh37
NC_000015.8:g.89366658_89366659delinsGC	NCBI36
NG_012162.1:g.5179_5180delinsGC , LRG_884:g.5179_5180delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-176_-175delinsGC MANE Select	ENSP00000327650.4:n.-176_-175delinsGC
ENST00000643536.1:c.-176_-175delinsGC	ENSP00000494429.1:n.-176_-175delinsGC
ENST00000333371.7:c.-176_-175delinsGC	ENSP00000327650.3:n.-176_-175delinsGC
ENST00000535906.1:c.-176_-175delinsGC	ENSP00000444053.1:n.-176_-175delinsGC
ENST00000556096.6:n.179_180delinsGC
ENST00000557358.1:n.172_173delinsGC
ENST00000574755.5:c.-176_-175delinsGC	ENSP00000460413.1:n.-176_-175delinsGC
NM_001289148.1:c.-176_-175delinsGC	NP_001276077.1:n.-176_-175delinsGC
NM_001289149.1:c.-387_-386delinsGC	NP_001276078.1:n.-387_-386delinsGC
NM_018668.4:c.-176_-175delinsGC , LRG_884t1:c.-176_-175delinsGC	NP_061138.3:n.-176_-175delinsGC
XM_005254884.2:c.-176_-175delinsGC	XP_005254941.1:n.-176_-175delinsGC
XM_005254887.1:c.-306_-305delinsGC	XP_005254944.1:n.-306_-305delinsGC
XM_005254888.2:c.-176_-175delinsGC	XP_005254945.1:n.-176_-175delinsGC
XM_011521448.1:c.-489_-488delinsGC	XP_011519750.1:n.-489_-488delinsGC
XM_017022075.2:c.-537_-536delinsGC	XP_016877564.1:n.-537_-536delinsGC
XM_017022076.1:c.-394_-393delinsGC	XP_016877565.1:n.-394_-393delinsGC
XR_001751213.2:n.161_162delinsGC
NM_018668.5:c.-176_-175delinsGC MANE Select	NP_061138.3:n.-176_-175delinsGC