Canonical Allele Identifier: CA2195398963

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002052G= , CM000677.2:g.91002052G=	GRCh38
NC_000015.9:g.91545282G= , CM000677.1:g.91545282G=	GRCh37
NC_000015.8:g.89346286G=	NCBI36
NG_012162.1:g.25552C= , LRG_884:g.25552C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1403C= MANE Select	ENSP00000327650.4:p.Ala468=
ENST00000643536.1:c.1403C=	ENSP00000494429.1:p.Ala468=
ENST00000647331.1:c.1403C=	ENSP00000493953.1:p.Ala468=
ENST00000333371.7:c.1403C=	ENSP00000327650.3:p.Ala468=
ENST00000535906.1:c.1322C=	ENSP00000444053.1:p.Ala441=
ENST00000574755.5:c.*1098C=	ENSP00000460413.1:n.*1098C=
NM_001289148.1:c.1322C=	NP_001276077.1:p.Ala441=
NM_001289149.1:c.1130C=	NP_001276078.1:p.Ala377=
NM_018668.4:c.1403C= , LRG_884t1:c.1403C=	NP_061138.3:p.Ala468=
XM_005254884.2:c.1325C=	XP_005254941.1:p.Ala442=
XM_005254887.1:c.1130C=	XP_005254944.1:p.Ala377=
XM_011521448.1:c.1130C=	XP_011519750.1:p.Ala377=
XM_011521449.1:c.1079C=	XP_011519751.1:p.Ala360=
XM_011521449.2:c.1079C=	XP_011519751.1:p.Ala360=
XM_017022075.2:c.1058C=	XP_016877564.1:p.Ala353=
XM_017022076.1:c.1058C=	XP_016877565.1:p.Ala353=
XR_001751213.2:n.1901C=
NM_018668.5:c.1403C= MANE Select	NP_061138.3:p.Ala468=