Canonical Allele Identifier: CA2630423736

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022399-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022401del , CM000677.2:g.91022401del	GRCh38
NC_000015.9:g.91565631del , CM000677.1:g.91565631del	GRCh37
NC_000015.8:g.89366635del	NCBI36
NG_012162.1:g.5204del , LRG_884:g.5204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-151del MANE Select	ENSP00000327650.4:n.-151del
ENST00000643536.1:c.-151del	ENSP00000494429.1:n.-151del
ENST00000333371.7:c.-151del	ENSP00000327650.3:n.-151del
ENST00000535906.1:c.-151del	ENSP00000444053.1:n.-151del
ENST00000556096.6:n.204del
ENST00000557358.1:n.197del
ENST00000574755.5:c.-151del	ENSP00000460413.1:n.-151del
NM_001289148.1:c.-151del	NP_001276077.1:n.-151del
NM_001289149.1:c.-362del	NP_001276078.1:n.-362del
NM_018668.4:c.-151del , LRG_884t1:c.-151del	NP_061138.3:n.-151del
XM_005254884.2:c.-151del	XP_005254941.1:n.-151del
XM_005254887.1:c.-281del	XP_005254944.1:n.-281del
XM_005254888.2:c.-151del	XP_005254945.1:n.-151del
XM_011521448.1:c.-464del	XP_011519750.1:n.-464del
XM_017022075.2:c.-512del	XP_016877564.1:n.-512del
XM_017022076.1:c.-369del	XP_016877565.1:n.-369del
XR_001751213.2:n.186del
NM_018668.5:c.-151del MANE Select	NP_061138.3:n.-151del