Canonical Allele Identifier: CA2630424366

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022513-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022514del , CM000677.2:g.91022514del	GRCh38
NC_000015.9:g.91565744del , CM000677.1:g.91565744del	GRCh37
NC_000015.8:g.89366748del	NCBI36
NG_012162.1:g.5090del , LRG_884:g.5090del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-265del MANE Select	ENSP00000327650.4:n.-265del
ENST00000643536.1:c.-265del	ENSP00000494429.1:n.-265del
ENST00000333371.7:c.-265del	ENSP00000327650.3:n.-265del
ENST00000535906.1:c.-265del	ENSP00000444053.1:n.-265del
ENST00000556096.6:n.90del
ENST00000557358.1:n.83del
NM_001289148.1:c.-265del	NP_001276077.1:n.-265del
NM_001289149.1:c.-476del	NP_001276078.1:n.-476del
NM_018668.4:c.-265del , LRG_884t1:c.-265del	NP_061138.3:n.-265del
XM_005254884.2:c.-265del	XP_005254941.1:n.-265del
XM_005254887.1:c.-395del	XP_005254944.1:n.-395del
XM_005254888.2:c.-265del	XP_005254945.1:n.-265del
XM_011521448.1:c.-578del	XP_011519750.1:n.-578del
XM_017022075.2:c.-626del	XP_016877564.1:n.-626del
XM_017022076.1:c.-483del	XP_016877565.1:n.-483del
XR_001751213.2:n.72del
NM_018668.5:c.-265del MANE Select	NP_061138.3:n.-265del