Canonical Allele Identifier: CA2195398966

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002063G= , CM000677.2:g.91002063G=	GRCh38
NC_000015.9:g.91545293G= , CM000677.1:g.91545293G=	GRCh37
NC_000015.8:g.89346297G=	NCBI36
NG_012162.1:g.25541C= , LRG_884:g.25541C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1392C= MANE Select	ENSP00000327650.4:p.Thr464=
ENST00000643536.1:c.1392C=	ENSP00000494429.1:p.Thr464=
ENST00000647331.1:c.1392C=	ENSP00000493953.1:p.Thr464=
ENST00000333371.7:c.1392C=	ENSP00000327650.3:p.Thr464=
ENST00000535906.1:c.1311C=	ENSP00000444053.1:p.Thr437=
ENST00000574755.5:c.*1087C=	ENSP00000460413.1:n.*1087C=
NM_001289148.1:c.1311C=	NP_001276077.1:p.Thr437=
NM_001289149.1:c.1119C=	NP_001276078.1:p.Thr373=
NM_018668.4:c.1392C= , LRG_884t1:c.1392C=	NP_061138.3:p.Thr464=
XM_005254884.2:c.1314C=	XP_005254941.1:p.Thr438=
XM_005254887.1:c.1119C=	XP_005254944.1:p.Thr373=
XM_011521448.1:c.1119C=	XP_011519750.1:p.Thr373=
XM_011521449.1:c.1068C=	XP_011519751.1:p.Thr356=
XM_011521449.2:c.1068C=	XP_011519751.1:p.Thr356=
XM_017022075.2:c.1047C=	XP_016877564.1:p.Thr349=
XM_017022076.1:c.1047C=	XP_016877565.1:p.Thr349=
XR_001751213.2:n.1890C=
NM_018668.5:c.1392C= MANE Select	NP_061138.3:p.Thr464=