Canonical Allele Identifier: CA2195408556

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022583A= , CM000677.2:g.91022583A=	GRCh38
NC_000015.9:g.91565813A= , CM000677.1:g.91565813A=	GRCh37
NC_000015.8:g.89366817A=	NCBI36
NG_012162.1:g.5021T= , LRG_884:g.5021T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-334T= MANE Select	ENSP00000327650.4:n.-334T=
ENST00000333371.7:c.-334T=	ENSP00000327650.3:n.-334T=
ENST00000535906.1:c.-334T=	ENSP00000444053.1:n.-334T=
ENST00000556096.6:n.21T=
ENST00000557358.1:n.14T=
NM_001289148.1:c.-334T=	NP_001276077.1:n.-334T=
NM_001289149.1:c.-545T=	NP_001276078.1:n.-545T=
NM_018668.4:c.-334T= , LRG_884t1:c.-334T=	NP_061138.3:n.-334T=
XM_005254884.2:c.-334T=	XP_005254941.1:n.-334T=
XM_005254887.1:c.-464T=	XP_005254944.1:n.-464T=
XM_005254888.2:c.-334T=	XP_005254945.1:n.-334T=
XM_011521448.1:c.-647T=	XP_011519750.1:n.-647T=
XM_017022075.2:c.-695T=	XP_016877564.1:n.-695T=
XM_017022076.1:c.-552T=	XP_016877565.1:n.-552T=
XR_001751213.2:n.3T=
NM_018668.5:c.-334T= MANE Select	NP_061138.3:n.-334T=