Canonical Allele Identifier: CA2630424625

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022550-CGTACGAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022551_91022558del , CM000677.2:g.91022551_91022558del	GRCh38
NC_000015.9:g.91565781_91565788del , CM000677.1:g.91565781_91565788del	GRCh37
NC_000015.8:g.89366785_89366792del	NCBI36
NG_012162.1:g.5046_5053del , LRG_884:g.5046_5053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-309_-302del MANE Select	ENSP00000327650.4:n.-309_-302del
ENST00000643536.1:c.-309_-302del	ENSP00000494429.1:n.-309_-302del
ENST00000333371.7:c.-309_-302del	ENSP00000327650.3:n.-309_-302del
ENST00000535906.1:c.-309_-302del	ENSP00000444053.1:n.-309_-302del
ENST00000556096.6:n.46_53del
ENST00000557358.1:n.39_46del
NM_001289148.1:c.-309_-302del	NP_001276077.1:n.-309_-302del
NM_001289149.1:c.-520_-513del	NP_001276078.1:n.-520_-513del
NM_018668.4:c.-309_-302del , LRG_884t1:c.-309_-302del	NP_061138.3:n.-309_-302del
XM_005254884.2:c.-309_-302del	XP_005254941.1:n.-309_-302del
XM_005254887.1:c.-439_-432del	XP_005254944.1:n.-439_-432del
XM_005254888.2:c.-309_-302del	XP_005254945.1:n.-309_-302del
XM_011521448.1:c.-622_-615del	XP_011519750.1:n.-622_-615del
XM_017022075.2:c.-670_-663del	XP_016877564.1:n.-670_-663del
XM_017022076.1:c.-527_-520del	XP_016877565.1:n.-527_-520del
XR_001751213.2:n.28_35del
NM_018668.5:c.-309_-302del MANE Select	NP_061138.3:n.-309_-302del