Canonical Allele Identifier: CA2195408560

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022589G= , CM000677.2:g.91022589G=	GRCh38
NC_000015.9:g.91565819G= , CM000677.1:g.91565819G=	GRCh37
NC_000015.8:g.89366823G=	NCBI36
NG_012162.1:g.5015C= , LRG_884:g.5015C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-340C= MANE Select	ENSP00000327650.4:n.-340C=
ENST00000333371.7:c.-340C=	ENSP00000327650.3:n.-340C=
ENST00000535906.1:c.-340C=	ENSP00000444053.1:n.-340C=
ENST00000556096.6:n.15C=
ENST00000557358.1:n.8C=
NM_001289148.1:c.-340C=	NP_001276077.1:n.-340C=
NM_001289149.1:c.-551C=	NP_001276078.1:n.-551C=
NM_018668.4:c.-340C= , LRG_884t1:c.-340C=	NP_061138.3:n.-340C=
XM_005254887.1:c.-470C=	XP_005254944.1:n.-470C=
XM_011521448.1:c.-653C=	XP_011519750.1:n.-653C=
XM_017022075.2:c.-701C=	XP_016877564.1:n.-701C=
XM_017022076.1:c.-558C=	XP_016877565.1:n.-558C=
NM_018668.5:c.-340C= MANE Select	NP_061138.3:n.-340C=