Canonical Allele Identifier: CA2195398962

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002050C= , CM000677.2:g.91002050C=	GRCh38
NC_000015.9:g.91545280C= , CM000677.1:g.91545280C=	GRCh37
NC_000015.8:g.89346284C=	NCBI36
NG_012162.1:g.25554G= , LRG_884:g.25554G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1405G= MANE Select	ENSP00000327650.4:p.Gly469=
ENST00000643536.1:c.1405G=	ENSP00000494429.1:p.Gly469=
ENST00000647331.1:c.1405G=	ENSP00000493953.1:p.Gly469=
ENST00000333371.7:c.1405G=	ENSP00000327650.3:p.Gly469=
ENST00000535906.1:c.1324G=	ENSP00000444053.1:p.Gly442=
ENST00000574755.5:c.*1100G=	ENSP00000460413.1:n.*1100G=
NM_001289148.1:c.1324G=	NP_001276077.1:p.Gly442=
NM_001289149.1:c.1132G=	NP_001276078.1:p.Gly378=
NM_018668.4:c.1405G= , LRG_884t1:c.1405G=	NP_061138.3:p.Gly469=
XM_005254884.2:c.1327G=	XP_005254941.1:p.Gly443=
XM_005254887.1:c.1132G=	XP_005254944.1:p.Gly378=
XM_011521448.1:c.1132G=	XP_011519750.1:p.Gly378=
XM_011521449.1:c.1081G=	XP_011519751.1:p.Gly361=
XM_011521449.2:c.1081G=	XP_011519751.1:p.Gly361=
XM_017022075.2:c.1060G=	XP_016877564.1:p.Gly354=
XM_017022076.1:c.1060G=	XP_016877565.1:p.Gly354=
XR_001751213.2:n.1903G=
NM_018668.5:c.1405G= MANE Select	NP_061138.3:p.Gly469=