Canonical Allele Identifier: CA2630425189

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91001962-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91001964del , CM000677.2:g.91001964del	GRCh38
NC_000015.9:g.91545194del , CM000677.1:g.91545194del	GRCh37
NC_000015.8:g.89346198del	NCBI36
NG_012162.1:g.25641del , LRG_884:g.25641del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1405+87del MANE Select	ENSP00000327650.4:n.1405+87del
ENST00000643536.1:c.1405+87del	ENSP00000494429.1:n.1405+87del
ENST00000647331.1:c.1405+87del	ENSP00000493953.1:n.1405+87del
ENST00000333371.7:c.1405+87del	ENSP00000327650.3:n.1405+87del
ENST00000535906.1:c.1324+87del	ENSP00000444053.1:n.1324+87del
ENST00000574755.5:c.*1100+87del	ENSP00000460413.1:n.*1100+87del
NM_001289148.1:c.1324+87del	NP_001276077.1:n.1324+87del
NM_001289149.1:c.1132+87del	NP_001276078.1:n.1132+87del
NM_018668.4:c.1405+87del , LRG_884t1:c.1405+87del	NP_061138.3:n.1405+87del
XM_005254884.2:c.1327+87del	XP_005254941.1:n.1327+87del
XM_005254887.1:c.1132+87del	XP_005254944.1:n.1132+87del
XM_011521448.1:c.1132+87del	XP_011519750.1:n.1132+87del
XM_011521449.1:c.1081+87del	XP_011519751.1:n.1081+87del
XM_011521449.2:c.1081+87del	XP_011519751.1:n.1081+87del
XM_017022075.2:c.1060+87del	XP_016877564.1:n.1060+87del
XM_017022076.1:c.1060+87del	XP_016877565.1:n.1060+87del
XR_001751213.2:n.1903+87del
NM_018668.5:c.1405+87del MANE Select	NP_061138.3:n.1405+87del