Canonical Allele Identifier: CA2195408550

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022575C= , CM000677.2:g.91022575C=	GRCh38
NC_000015.9:g.91565805C= , CM000677.1:g.91565805C=	GRCh37
NC_000015.8:g.89366809C=	NCBI36
NG_012162.1:g.5029G= , LRG_884:g.5029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-326G= MANE Select	ENSP00000327650.4:n.-326G=
ENST00000333371.7:c.-326G=	ENSP00000327650.3:n.-326G=
ENST00000535906.1:c.-326G=	ENSP00000444053.1:n.-326G=
ENST00000556096.6:n.29G=
ENST00000557358.1:n.22G=
NM_001289148.1:c.-326G=	NP_001276077.1:n.-326G=
NM_001289149.1:c.-537G=	NP_001276078.1:n.-537G=
NM_018668.4:c.-326G= , LRG_884t1:c.-326G=	NP_061138.3:n.-326G=
XM_005254884.2:c.-326G=	XP_005254941.1:n.-326G=
XM_005254887.1:c.-456G=	XP_005254944.1:n.-456G=
XM_005254888.2:c.-326G=	XP_005254945.1:n.-326G=
XM_011521448.1:c.-639G=	XP_011519750.1:n.-639G=
XM_017022075.2:c.-687G=	XP_016877564.1:n.-687G=
XM_017022076.1:c.-544G=	XP_016877565.1:n.-544G=
XR_001751213.2:n.11G=
NM_018668.5:c.-326G= MANE Select	NP_061138.3:n.-326G=