Canonical Allele Identifier: CA2195404749

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91014531C= , CM000677.2:g.91014531C=	GRCh38
NC_000015.9:g.91557761C= , CM000677.1:g.91557761C=	GRCh37
NC_000015.8:g.89358765C=	NCBI36
NG_012162.1:g.13073G= , LRG_884:g.13073G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.240-98G= MANE Select	ENSP00000327650.4:n.240-98G=
ENST00000643536.1:c.240-98G=	ENSP00000494429.1:n.240-98G=
ENST00000647331.1:c.240-98G=	ENSP00000493953.1:n.240-98G=
ENST00000333371.7:c.240-98G=	ENSP00000327650.3:n.240-98G=
ENST00000535906.1:c.159-98G=	ENSP00000444053.1:n.159-98G=
ENST00000554264.5:n.163-98G=
ENST00000556096.6:n.634-98G=
ENST00000557358.1:n.444-98G=
ENST00000574755.5:c.178-98G=	ENSP00000460413.1:n.178-98G=
NM_001289148.1:c.159-98G=	NP_001276077.1:n.159-98G=
NM_001289149.1:c.-34-98G=	NP_001276078.1:n.-34-98G=
NM_018668.4:c.240-98G= , LRG_884t1:c.240-98G=	NP_061138.3:n.240-98G=
XM_005254884.2:c.240-98G=	XP_005254941.1:n.240-98G=
XM_005254887.1:c.-34-98G=	XP_005254944.1:n.-34-98G=
XM_005254888.2:c.240-98G=	XP_005254945.1:n.240-98G=
XM_011521448.1:c.-34-98G=	XP_011519750.1:n.-34-98G=
XM_017022075.2:c.-122-98G=	XP_016877564.1:n.-122-98G=
XM_017022076.1:c.-122-98G=	XP_016877565.1:n.-122-98G=
XR_001751213.2:n.576-98G=
NM_018668.5:c.240-98G= MANE Select	NP_061138.3:n.240-98G=