Canonical Allele Identifier: CA2630423449

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022360-TCCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022361_91022364del , CM000677.2:g.91022361_91022364del	GRCh38
NC_000015.9:g.91565591_91565594del , CM000677.1:g.91565591_91565594del	GRCh37
NC_000015.8:g.89366595_89366598del	NCBI36
NG_012162.1:g.5240_5243del , LRG_884:g.5240_5243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-115_-112del MANE Select	ENSP00000327650.4:n.-115_-112del
ENST00000643536.1:c.-115_-112del	ENSP00000494429.1:n.-115_-112del
ENST00000333371.7:c.-115_-112del	ENSP00000327650.3:n.-115_-112del
ENST00000535906.1:c.-115_-112del	ENSP00000444053.1:n.-115_-112del
ENST00000556096.6:n.240_243del
ENST00000557358.1:n.233_236del
ENST00000574755.5:c.-115_-112del	ENSP00000460413.1:n.-115_-112del
NM_001289148.1:c.-115_-112del	NP_001276077.1:n.-115_-112del
NM_001289149.1:c.-326_-323del	NP_001276078.1:n.-326_-323del
NM_018668.4:c.-115_-112del , LRG_884t1:c.-115_-112del	NP_061138.3:n.-115_-112del
XM_005254884.2:c.-115_-112del	XP_005254941.1:n.-115_-112del
XM_005254887.1:c.-245_-242del	XP_005254944.1:n.-245_-242del
XM_005254888.2:c.-115_-112del	XP_005254945.1:n.-115_-112del
XM_011521448.1:c.-428_-425del	XP_011519750.1:n.-428_-425del
XM_017022075.2:c.-476_-473del	XP_016877564.1:n.-476_-473del
XM_017022076.1:c.-333_-330del	XP_016877565.1:n.-333_-330del
XR_001751213.2:n.222_225del
NM_018668.5:c.-115_-112del MANE Select	NP_061138.3:n.-115_-112del