Canonical Allele Identifier: CA2195408559

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022588C= , CM000677.2:g.91022588C=	GRCh38
NC_000015.9:g.91565818C= , CM000677.1:g.91565818C=	GRCh37
NC_000015.8:g.89366822C=	NCBI36
NG_012162.1:g.5016G= , LRG_884:g.5016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-339G= MANE Select	ENSP00000327650.4:n.-339G=
ENST00000333371.7:c.-339G=	ENSP00000327650.3:n.-339G=
ENST00000535906.1:c.-339G=	ENSP00000444053.1:n.-339G=
ENST00000556096.6:n.16G=
ENST00000557358.1:n.9G=
NM_001289148.1:c.-339G=	NP_001276077.1:n.-339G=
NM_001289149.1:c.-550G=	NP_001276078.1:n.-550G=
NM_018668.4:c.-339G= , LRG_884t1:c.-339G=	NP_061138.3:n.-339G=
XM_005254887.1:c.-469G=	XP_005254944.1:n.-469G=
XM_011521448.1:c.-652G=	XP_011519750.1:n.-652G=
XM_017022075.2:c.-700G=	XP_016877564.1:n.-700G=
XM_017022076.1:c.-557G=	XP_016877565.1:n.-557G=
NM_018668.5:c.-339G= MANE Select	NP_061138.3:n.-339G=