Canonical Allele Identifier: CA2195408460

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022413G= , CM000677.2:g.91022413G=	GRCh38
NC_000015.9:g.91565643G= , CM000677.1:g.91565643G=	GRCh37
NC_000015.8:g.89366647G=	NCBI36
NG_012162.1:g.5191C= , LRG_884:g.5191C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-164C= MANE Select	ENSP00000327650.4:n.-164C=
ENST00000643536.1:c.-164C=	ENSP00000494429.1:n.-164C=
ENST00000333371.7:c.-164C=	ENSP00000327650.3:n.-164C=
ENST00000535906.1:c.-164C=	ENSP00000444053.1:n.-164C=
ENST00000556096.6:n.191C=
ENST00000557358.1:n.184C=
ENST00000574755.5:c.-164C=	ENSP00000460413.1:n.-164C=
NM_001289148.1:c.-164C=	NP_001276077.1:n.-164C=
NM_001289149.1:c.-375C=	NP_001276078.1:n.-375C=
NM_018668.4:c.-164C= , LRG_884t1:c.-164C=	NP_061138.3:n.-164C=
XM_005254884.2:c.-164C=	XP_005254941.1:n.-164C=
XM_005254887.1:c.-294C=	XP_005254944.1:n.-294C=
XM_005254888.2:c.-164C=	XP_005254945.1:n.-164C=
XM_011521448.1:c.-477C=	XP_011519750.1:n.-477C=
XM_017022075.2:c.-525C=	XP_016877564.1:n.-525C=
XM_017022076.1:c.-382C=	XP_016877565.1:n.-382C=
XR_001751213.2:n.173C=
NM_018668.5:c.-164C= MANE Select	NP_061138.3:n.-164C=