Canonical Allele Identifier: CA2630422930

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022244-AGCCATGGCAGCGGTCACCTGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022248_91022268del , CM000677.2:g.91022248_91022268del	GRCh38
NC_000015.9:g.91565478_91565498del , CM000677.1:g.91565478_91565498del	GRCh37
NC_000015.8:g.89366482_89366502del	NCBI36
NG_012162.1:g.5339_5359del , LRG_884:g.5339_5359del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-16_5del
ENST00000643536.1:c.-16_5del
ENST00000647331.1:c.-16_5del
ENST00000333371.7:c.-16_5del
ENST00000535906.1:c.-16_5del
ENST00000556096.6:n.339_359del
ENST00000557358.1:n.332_352del
ENST00000574755.5:c.-16_5del
NM_001289148.1:c.-16_5del
NM_001289149.1:c.-227_-207del	NP_001276078.1:n.-227_-207del
NM_018668.4:c.-16_5del , LRG_884t1:c.-16_5del
XM_005254884.2:c.-16_5del
XM_005254887.1:c.-146_-126del	XP_005254944.1:n.-146_-126del
XM_005254888.2:c.-16_5del
XM_011521448.1:c.-329_-309del	XP_011519750.1:n.-329_-309del
XM_017022075.2:c.-377_-357del	XP_016877564.1:n.-377_-357del
XM_017022076.1:c.-234_-214del	XP_016877565.1:n.-234_-214del
XR_001751213.2:n.321_341del
NM_018668.5:c.-16_5del