Canonical Allele Identifier: CA7745251

Gene: VPS33B

Linked Data

• dbSNP Id: rs757689025
• ExAC: 15:91565524 CT / C
• gnomAD v2: 15-91565524-CT-C
• gnomAD v4: 15-91022294-CT-C
• MyVariant Identifiers: chr15:g.91565525del (hg19) ; chr15:g.91022295del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022295del , CM000677.2:g.91022295del	GRCh38
NC_000015.9:g.91565525del , CM000677.1:g.91565525del	GRCh37
NC_000015.8:g.89366529del	NCBI36
NG_012162.1:g.5309del , LRG_884:g.5309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-46del MANE Select	ENSP00000327650.4:n.-46del
ENST00000643536.1:c.-46del	ENSP00000494429.1:n.-46del
ENST00000333371.7:c.-46del	ENSP00000327650.3:n.-46del
ENST00000535906.1:c.-46del	ENSP00000444053.1:n.-46del
ENST00000556096.6:n.309del
ENST00000557358.1:n.302del
ENST00000574755.5:c.-46del	ENSP00000460413.1:n.-46del
NM_001289148.1:c.-46del	NP_001276077.1:n.-46del
NM_001289149.1:c.-257del	NP_001276078.1:n.-257del
NM_018668.4:c.-46del , LRG_884t1:c.-46del	NP_061138.3:n.-46del
XM_005254884.2:c.-46del	XP_005254941.1:n.-46del
XM_005254887.1:c.-176del	XP_005254944.1:n.-176del
XM_005254888.2:c.-46del	XP_005254945.1:n.-46del
XM_011521448.1:c.-359del	XP_011519750.1:n.-359del
XM_017022075.2:c.-407del	XP_016877564.1:n.-407del
XM_017022076.1:c.-264del	XP_016877565.1:n.-264del
XR_001751213.2:n.291del
NM_018668.5:c.-46del MANE Select	NP_061138.3:n.-46del