Canonical Allele Identifier: CA2805218300

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022475T>A , CM000677.2:g.91022475T>A	GRCh38
NC_000015.9:g.91565705T>A , CM000677.1:g.91565705T>A	GRCh37
NC_000015.8:g.89366709T>A	NCBI36
NG_012162.1:g.5129A>T , LRG_884:g.5129A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-226A>T MANE Select	ENSP00000327650.4:n.-226A>T
ENST00000643536.1:c.-226A>T	ENSP00000494429.1:n.-226A>T
ENST00000333371.7:c.-226A>T	ENSP00000327650.3:n.-226A>T
ENST00000535906.1:c.-226A>T	ENSP00000444053.1:n.-226A>T
ENST00000556096.6:n.129A>T
ENST00000557358.1:n.122A>T
ENST00000574755.5:c.-226A>T	ENSP00000460413.1:n.-226A>T
NM_001289148.1:c.-226A>T	NP_001276077.1:n.-226A>T
NM_001289149.1:c.-437A>T	NP_001276078.1:n.-437A>T
NM_018668.4:c.-226A>T , LRG_884t1:c.-226A>T	NP_061138.3:n.-226A>T
XM_005254884.2:c.-226A>T	XP_005254941.1:n.-226A>T
XM_005254887.1:c.-356A>T	XP_005254944.1:n.-356A>T
XM_005254888.2:c.-226A>T	XP_005254945.1:n.-226A>T
XM_011521448.1:c.-539A>T	XP_011519750.1:n.-539A>T
XM_017022075.2:c.-587A>T	XP_016877564.1:n.-587A>T
XM_017022076.1:c.-444A>T	XP_016877565.1:n.-444A>T
XR_001751213.2:n.111A>T
NM_018668.5:c.-226A>T MANE Select	NP_061138.3:n.-226A>T