Canonical Allele Identifier: CA2195408434

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022367A= , CM000677.2:g.91022367A=	GRCh38
NC_000015.9:g.91565597A= , CM000677.1:g.91565597A=	GRCh37
NC_000015.8:g.89366601A=	NCBI36
NG_012162.1:g.5237T= , LRG_884:g.5237T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-118T= MANE Select	ENSP00000327650.4:n.-118T=
ENST00000643536.1:c.-118T=	ENSP00000494429.1:n.-118T=
ENST00000333371.7:c.-118T=	ENSP00000327650.3:n.-118T=
ENST00000535906.1:c.-118T=	ENSP00000444053.1:n.-118T=
ENST00000556096.6:n.237T=
ENST00000557358.1:n.230T=
ENST00000574755.5:c.-118T=	ENSP00000460413.1:n.-118T=
NM_001289148.1:c.-118T=	NP_001276077.1:n.-118T=
NM_001289149.1:c.-329T=	NP_001276078.1:n.-329T=
NM_018668.4:c.-118T= , LRG_884t1:c.-118T=	NP_061138.3:n.-118T=
XM_005254884.2:c.-118T=	XP_005254941.1:n.-118T=
XM_005254887.1:c.-248T=	XP_005254944.1:n.-248T=
XM_005254888.2:c.-118T=	XP_005254945.1:n.-118T=
XM_011521448.1:c.-431T=	XP_011519750.1:n.-431T=
XM_017022075.2:c.-479T=	XP_016877564.1:n.-479T=
XM_017022076.1:c.-336T=	XP_016877565.1:n.-336T=
XR_001751213.2:n.219T=
NM_018668.5:c.-118T= MANE Select	NP_061138.3:n.-118T=