Canonical Allele Identifier: CA2195398964

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002056C= , CM000677.2:g.91002056C=	GRCh38
NC_000015.9:g.91545286C= , CM000677.1:g.91545286C=	GRCh37
NC_000015.8:g.89346290C=	NCBI36
NG_012162.1:g.25548G= , LRG_884:g.25548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1399G= MANE Select	ENSP00000327650.4:p.Ala467=
ENST00000643536.1:c.1399G=	ENSP00000494429.1:p.Ala467=
ENST00000647331.1:c.1399G=	ENSP00000493953.1:p.Ala467=
ENST00000333371.7:c.1399G=	ENSP00000327650.3:p.Ala467=
ENST00000535906.1:c.1318G=	ENSP00000444053.1:p.Ala440=
ENST00000574755.5:c.*1094G=	ENSP00000460413.1:n.*1094G=
NM_001289148.1:c.1318G=	NP_001276077.1:p.Ala440=
NM_001289149.1:c.1126G=	NP_001276078.1:p.Ala376=
NM_018668.4:c.1399G= , LRG_884t1:c.1399G=	NP_061138.3:p.Ala467=
XM_005254884.2:c.1321G=	XP_005254941.1:p.Ala441=
XM_005254887.1:c.1126G=	XP_005254944.1:p.Ala376=
XM_011521448.1:c.1126G=	XP_011519750.1:p.Ala376=
XM_011521449.1:c.1075G=	XP_011519751.1:p.Ala359=
XM_011521449.2:c.1075G=	XP_011519751.1:p.Ala359=
XM_017022075.2:c.1054G=	XP_016877564.1:p.Ala352=
XM_017022076.1:c.1054G=	XP_016877565.1:p.Ala352=
XR_001751213.2:n.1897G=
NM_018668.5:c.1399G= MANE Select	NP_061138.3:p.Ala467=