Canonical Allele Identifier: CA7744577

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90999966G>A , CM000677.2:g.90999966G>A	GRCh38
NC_000015.9:g.91543196G>A , CM000677.1:g.91543196G>A	GRCh37
NC_000015.8:g.89344200G>A	NCBI36
NG_012162.1:g.27638C>T , LRG_884:g.27638C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1591C>T MANE Select	ENSP00000327650.4:p.Arg531Trp
ENST00000643536.1:c.1591C>T	ENSP00000494429.1:p.Arg531Trp
ENST00000647331.1:c.1591C>T	ENSP00000493953.1:p.Arg531Trp
ENST00000333371.7:c.1591C>T	ENSP00000327650.3:p.Arg531Trp
ENST00000535906.1:c.1510C>T	ENSP00000444053.1:p.Arg504Trp
ENST00000554660.1:n.526C>T
ENST00000557470.5:n.147+524C>T
ENST00000574755.5:c.*1286C>T	ENSP00000460413.1:n.*1286C>T
NM_001289148.1:c.1510C>T	NP_001276077.1:p.Arg504Trp
NM_001289149.1:c.1318C>T	NP_001276078.1:p.Arg440Trp
NM_018668.4:c.1591C>T , LRG_884t1:c.1591C>T	NP_061138.3:p.Arg531Trp
XM_005254884.2:c.1513C>T	XP_005254941.1:p.Arg505Trp
XM_005254887.1:c.1318C>T	XP_005254944.1:p.Arg440Trp
XM_011521448.1:c.1318C>T	XP_011519750.1:p.Arg440Trp
XM_011521449.1:c.1267C>T	XP_011519751.1:p.Arg423Trp
XM_011521449.2:c.1267C>T	XP_011519751.1:p.Arg423Trp
XM_017022075.2:c.1246C>T	XP_016877564.1:p.Arg416Trp
XM_017022076.1:c.1246C>T	XP_016877565.1:p.Arg416Trp
XR_001751213.2:n.2089C>T
NM_018668.5:c.1591C>T MANE Select	NP_061138.3:p.Arg531Trp