Canonical Allele Identifier: CA203118

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91013804C>T , CM000677.2:g.91013804C>T	GRCh38
NC_000015.9:g.91557034C>T , CM000677.1:g.91557034C>T	GRCh37
NC_000015.8:g.89358038C>T	NCBI36
NG_012162.1:g.13800G>A , LRG_884:g.13800G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.357G>A MANE Select	ENSP00000327650.4:p.Lys119=
ENST00000643536.1:c.357G>A	ENSP00000494429.1:p.Lys119=
ENST00000647331.1:c.357G>A	ENSP00000493953.1:p.Lys119=
ENST00000333371.7:c.357G>A	ENSP00000327650.3:p.Lys119=
ENST00000535906.1:c.276G>A	ENSP00000444053.1:p.Lys92=
ENST00000554264.5:n.280G>A
ENST00000556096.6:n.751G>A
ENST00000557358.1:n.561G>A
ENST00000574755.5:c.*52G>A	ENSP00000460413.1:n.*52G>A
NM_001289148.1:c.276G>A	NP_001276077.1:p.Lys92=
NM_001289149.1:c.84G>A	NP_001276078.1:p.Lys28=
NM_018668.4:c.357G>A , LRG_884t1:c.357G>A	NP_061138.3:p.Lys119=
XM_005254884.2:c.357G>A	XP_005254941.1:p.Lys119=
XM_005254887.1:c.84G>A	XP_005254944.1:p.Lys28=
XM_005254888.2:c.357G>A	XP_005254945.1:p.Lys119=
XM_011521448.1:c.84G>A	XP_011519750.1:p.Lys28=
XM_017022075.2:c.-5G>A	XP_016877564.1:n.-5G>A
XM_017022076.1:c.-5G>A	XP_016877565.1:n.-5G>A
XR_001751213.2:n.693G>A
NM_018668.5:c.357G>A MANE Select	NP_061138.3:p.Lys119=