Canonical Allele Identifier: CA2195408383

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022260A= , CM000677.2:g.91022260A=	GRCh38
NC_000015.9:g.91565490A= , CM000677.1:g.91565490A=	GRCh37
NC_000015.8:g.89366494A=	NCBI36
NG_012162.1:g.5344T= , LRG_884:g.5344T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-11T= MANE Select	ENSP00000327650.4:n.-11T=
ENST00000643536.1:c.-11T=	ENSP00000494429.1:n.-11T=
ENST00000647331.1:c.-11T=	ENSP00000493953.1:n.-11T=
ENST00000333371.7:c.-11T=	ENSP00000327650.3:n.-11T=
ENST00000535906.1:c.-11T=	ENSP00000444053.1:n.-11T=
ENST00000556096.6:n.344T=
ENST00000557358.1:n.337T=
ENST00000574755.5:c.-11T=	ENSP00000460413.1:n.-11T=
NM_001289148.1:c.-11T=	NP_001276077.1:n.-11T=
NM_001289149.1:c.-222T=	NP_001276078.1:n.-222T=
NM_018668.4:c.-11T= , LRG_884t1:c.-11T=	NP_061138.3:n.-11T=
XM_005254884.2:c.-11T=	XP_005254941.1:n.-11T=
XM_005254887.1:c.-141T=	XP_005254944.1:n.-141T=
XM_005254888.2:c.-11T=	XP_005254945.1:n.-11T=
XM_011521448.1:c.-324T=	XP_011519750.1:n.-324T=
XM_017022075.2:c.-372T=	XP_016877564.1:n.-372T=
XM_017022076.1:c.-229T=	XP_016877565.1:n.-229T=
XR_001751213.2:n.326T=
NM_018668.5:c.-11T= MANE Select	NP_061138.3:n.-11T=