Canonical Allele Identifier: CA656693537

Gene: VPS33B

Linked Data

• COSMIC: COSN16857101

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022355_91022356insT , CM000677.2:g.91022355_91022356insT	GRCh38
NC_000015.9:g.91565585_91565586insT , CM000677.1:g.91565585_91565586insT	GRCh37
NC_000015.8:g.89366589_89366590insT	NCBI36
NG_012162.1:g.5248_5249insA , LRG_884:g.5248_5249insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-107_-106insA MANE Select	ENSP00000327650.4:n.-107_-106insA
ENST00000643536.1:c.-107_-106insA	ENSP00000494429.1:n.-107_-106insA
ENST00000333371.7:c.-107_-106insA	ENSP00000327650.3:n.-107_-106insA
ENST00000535906.1:c.-107_-106insA	ENSP00000444053.1:n.-107_-106insA
ENST00000556096.6:n.248_249insA
ENST00000557358.1:n.241_242insA
ENST00000574755.5:c.-107_-106insA	ENSP00000460413.1:n.-107_-106insA
NM_001289148.1:c.-107_-106insA	NP_001276077.1:n.-107_-106insA
NM_001289149.1:c.-318_-317insA	NP_001276078.1:n.-318_-317insA
NM_018668.4:c.-107_-106insA , LRG_884t1:c.-107_-106insA	NP_061138.3:n.-107_-106insA
XM_005254884.2:c.-107_-106insA	XP_005254941.1:n.-107_-106insA
XM_005254887.1:c.-237_-236insA	XP_005254944.1:n.-237_-236insA
XM_005254888.2:c.-107_-106insA	XP_005254945.1:n.-107_-106insA
XM_011521448.1:c.-420_-419insA	XP_011519750.1:n.-420_-419insA
XM_017022075.2:c.-468_-467insA	XP_016877564.1:n.-468_-467insA
XM_017022076.1:c.-325_-324insA	XP_016877565.1:n.-325_-324insA
XR_001751213.2:n.230_231insA
NM_018668.5:c.-107_-106insA MANE Select	NP_061138.3:n.-107_-106insA