Canonical Allele Identifier: CA2195398890

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91001907A= , CM000677.2:g.91001907A=	GRCh38
NC_000015.9:g.91545137A= , CM000677.1:g.91545137A=	GRCh37
NC_000015.8:g.89346141A=	NCBI36
NG_012162.1:g.25697T= , LRG_884:g.25697T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1405+143T= MANE Select	ENSP00000327650.4:n.1405+143T=
ENST00000643536.1:c.1405+143T=	ENSP00000494429.1:n.1405+143T=
ENST00000647331.1:c.1405+143T=	ENSP00000493953.1:n.1405+143T=
ENST00000333371.7:c.1405+143T=	ENSP00000327650.3:n.1405+143T=
ENST00000535906.1:c.1324+143T=	ENSP00000444053.1:n.1324+143T=
ENST00000574755.5:c.*1100+143T=	ENSP00000460413.1:n.*1100+143T=
NM_001289148.1:c.1324+143T=	NP_001276077.1:n.1324+143T=
NM_001289149.1:c.1132+143T=	NP_001276078.1:n.1132+143T=
NM_018668.4:c.1405+143T= , LRG_884t1:c.1405+143T=	NP_061138.3:n.1405+143T=
XM_005254884.2:c.1327+143T=	XP_005254941.1:n.1327+143T=
XM_005254887.1:c.1132+143T=	XP_005254944.1:n.1132+143T=
XM_011521448.1:c.1132+143T=	XP_011519750.1:n.1132+143T=
XM_011521449.1:c.1081+143T=	XP_011519751.1:n.1081+143T=
XM_011521449.2:c.1081+143T=	XP_011519751.1:n.1081+143T=
XM_017022075.2:c.1060+143T=	XP_016877564.1:n.1060+143T=
XM_017022076.1:c.1060+143T=	XP_016877565.1:n.1060+143T=
XR_001751213.2:n.1903+143T=
NM_018668.5:c.1405+143T= MANE Select	NP_061138.3:n.1405+143T=