Canonical Allele Identifier: CA2195398906

Gene: VPS33B

Linked Data

• dbSNP Id: rs2040450062

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91001955_91001963del , CM000677.2:g.91001955_91001963del	GRCh38
NC_000015.9:g.91545185_91545193del , CM000677.1:g.91545185_91545193del	GRCh37
NC_000015.8:g.89346189_89346197del	NCBI36
NG_012162.1:g.25645_25653del , LRG_884:g.25645_25653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1405+91_1405+99del MANE Select	ENSP00000327650.4:n.1405+91_1405+99del
ENST00000643536.1:c.1405+91_1405+99del	ENSP00000494429.1:n.1405+91_1405+99del
ENST00000647331.1:c.1405+91_1405+99del	ENSP00000493953.1:n.1405+91_1405+99del
ENST00000333371.7:c.1405+91_1405+99del	ENSP00000327650.3:n.1405+91_1405+99del
ENST00000535906.1:c.1324+91_1324+99del	ENSP00000444053.1:n.1324+91_1324+99del
ENST00000574755.5:c.*1100+91_*1100+99del	ENSP00000460413.1:n.*1100+91_*1100+99del
NM_001289148.1:c.1324+91_1324+99del	NP_001276077.1:n.1324+91_1324+99del
NM_001289149.1:c.1132+91_1132+99del	NP_001276078.1:n.1132+91_1132+99del
NM_018668.4:c.1405+91_1405+99del , LRG_884t1:c.1405+91_1405+99del	NP_061138.3:n.1405+91_1405+99del
XM_005254884.2:c.1327+91_1327+99del	XP_005254941.1:n.1327+91_1327+99del
XM_005254887.1:c.1132+91_1132+99del	XP_005254944.1:n.1132+91_1132+99del
XM_011521448.1:c.1132+91_1132+99del	XP_011519750.1:n.1132+91_1132+99del
XM_011521449.1:c.1081+91_1081+99del	XP_011519751.1:n.1081+91_1081+99del
XM_011521449.2:c.1081+91_1081+99del	XP_011519751.1:n.1081+91_1081+99del
XM_017022075.2:c.1060+91_1060+99del	XP_016877564.1:n.1060+91_1060+99del
XM_017022076.1:c.1060+91_1060+99del	XP_016877565.1:n.1060+91_1060+99del
XR_001751213.2:n.1903+91_1903+99del
NM_018668.5:c.1405+91_1405+99del MANE Select	NP_061138.3:n.1405+91_1405+99del