Canonical Allele Identifier: CA2195408553

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022577A= , CM000677.2:g.91022577A=	GRCh38
NC_000015.9:g.91565807A= , CM000677.1:g.91565807A=	GRCh37
NC_000015.8:g.89366811A=	NCBI36
NG_012162.1:g.5027T= , LRG_884:g.5027T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-328T= MANE Select	ENSP00000327650.4:n.-328T=
ENST00000333371.7:c.-328T=	ENSP00000327650.3:n.-328T=
ENST00000535906.1:c.-328T=	ENSP00000444053.1:n.-328T=
ENST00000556096.6:n.27T=
ENST00000557358.1:n.20T=
NM_001289148.1:c.-328T=	NP_001276077.1:n.-328T=
NM_001289149.1:c.-539T=	NP_001276078.1:n.-539T=
NM_018668.4:c.-328T= , LRG_884t1:c.-328T=	NP_061138.3:n.-328T=
XM_005254884.2:c.-328T=	XP_005254941.1:n.-328T=
XM_005254887.1:c.-458T=	XP_005254944.1:n.-458T=
XM_005254888.2:c.-328T=	XP_005254945.1:n.-328T=
XM_011521448.1:c.-641T=	XP_011519750.1:n.-641T=
XM_017022075.2:c.-689T=	XP_016877564.1:n.-689T=
XM_017022076.1:c.-546T=	XP_016877565.1:n.-546T=
XR_001751213.2:n.9T=
NM_018668.5:c.-328T= MANE Select	NP_061138.3:n.-328T=