Canonical Allele Identifier: CA2839421313

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002084dup , CM000677.2:g.91002084dup	GRCh38
NC_000015.9:g.91545314dup , CM000677.1:g.91545314dup	GRCh37
NC_000015.8:g.89346318dup	NCBI36
NG_012162.1:g.25520dup , LRG_884:g.25520dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1371dup MANE Select	ENSP00000327650.4:p.Lys458Ter
ENST00000643536.1:c.1371dup	ENSP00000494429.1:p.Lys458Ter
ENST00000647331.1:c.1371dup	ENSP00000493953.1:p.Lys458Ter
ENST00000333371.7:c.1371dup	ENSP00000327650.3:p.Lys458Ter
ENST00000535906.1:c.1290dup	ENSP00000444053.1:p.Lys431Ter
ENST00000574755.5:c.*1066dup	ENSP00000460413.1:n.*1066dup
NM_001289148.1:c.1290dup	NP_001276077.1:p.Lys431Ter
NM_001289149.1:c.1098dup	NP_001276078.1:p.Lys367Ter
NM_018668.4:c.1371dup , LRG_884t1:c.1371dup	NP_061138.3:p.Lys458Ter
XM_005254884.2:c.1293dup	XP_005254941.1:p.Lys432Ter
XM_005254887.1:c.1098dup	XP_005254944.1:p.Lys367Ter
XM_011521448.1:c.1098dup	XP_011519750.1:p.Lys367Ter
XM_011521449.1:c.1047dup	XP_011519751.1:p.Lys350Ter
XM_011521449.2:c.1047dup	XP_011519751.1:p.Lys350Ter
XM_017022075.2:c.1026dup	XP_016877564.1:p.Lys343Ter
XM_017022076.1:c.1026dup	XP_016877565.1:p.Lys343Ter
XR_001751213.2:n.1869dup
NM_018668.5:c.1371dup MANE Select	NP_061138.3:p.Lys458Ter