Canonical Allele Identifier: CA2630423178

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022276-GGAAGGACGCCCTTCGTTCTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022282_91022302del , CM000677.2:g.91022282_91022302del	GRCh38
NC_000015.9:g.91565512_91565532del , CM000677.1:g.91565512_91565532del	GRCh37
NC_000015.8:g.89366516_89366536del	NCBI36
NG_012162.1:g.5307_5327del , LRG_884:g.5307_5327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-48_-28del MANE Select	ENSP00000327650.4:n.-48_-28del
ENST00000643536.1:c.-48_-28del	ENSP00000494429.1:n.-48_-28del
ENST00000333371.7:c.-48_-28del	ENSP00000327650.3:n.-48_-28del
ENST00000535906.1:c.-48_-28del	ENSP00000444053.1:n.-48_-28del
ENST00000556096.6:n.307_327del
ENST00000557358.1:n.300_320del
ENST00000574755.5:c.-48_-28del	ENSP00000460413.1:n.-48_-28del
NM_001289148.1:c.-48_-28del	NP_001276077.1:n.-48_-28del
NM_001289149.1:c.-259_-239del	NP_001276078.1:n.-259_-239del
NM_018668.4:c.-48_-28del , LRG_884t1:c.-48_-28del	NP_061138.3:n.-48_-28del
XM_005254884.2:c.-48_-28del	XP_005254941.1:n.-48_-28del
XM_005254887.1:c.-178_-158del	XP_005254944.1:n.-178_-158del
XM_005254888.2:c.-48_-28del	XP_005254945.1:n.-48_-28del
XM_011521448.1:c.-361_-341del	XP_011519750.1:n.-361_-341del
XM_017022075.2:c.-409_-389del	XP_016877564.1:n.-409_-389del
XM_017022076.1:c.-266_-246del	XP_016877565.1:n.-266_-246del
XR_001751213.2:n.289_309del
NM_018668.5:c.-48_-28del MANE Select	NP_061138.3:n.-48_-28del