Canonical Allele Identifier: CA2805218292

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022279del , CM000677.2:g.91022279del	GRCh38
NC_000015.9:g.91565509del , CM000677.1:g.91565509del	GRCh37
NC_000015.8:g.89366513del	NCBI36
NG_012162.1:g.5326del , LRG_884:g.5326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-29del MANE Select	ENSP00000327650.4:n.-29del
ENST00000643536.1:c.-29del	ENSP00000494429.1:n.-29del
ENST00000647331.1:c.-29del	ENSP00000493953.1:n.-29del
ENST00000333371.7:c.-29del	ENSP00000327650.3:n.-29del
ENST00000535906.1:c.-29del	ENSP00000444053.1:n.-29del
ENST00000556096.6:n.326del
ENST00000557358.1:n.319del
ENST00000574755.5:c.-29del	ENSP00000460413.1:n.-29del
NM_001289148.1:c.-29del	NP_001276077.1:n.-29del
NM_001289149.1:c.-240del	NP_001276078.1:n.-240del
NM_018668.4:c.-29del , LRG_884t1:c.-29del	NP_061138.3:n.-29del
XM_005254884.2:c.-29del	XP_005254941.1:n.-29del
XM_005254887.1:c.-159del	XP_005254944.1:n.-159del
XM_005254888.2:c.-29del	XP_005254945.1:n.-29del
XM_011521448.1:c.-342del	XP_011519750.1:n.-342del
XM_017022075.2:c.-390del	XP_016877564.1:n.-390del
XM_017022076.1:c.-247del	XP_016877565.1:n.-247del
XR_001751213.2:n.308del
NM_018668.5:c.-29del MANE Select	NP_061138.3:n.-29del