Canonical Allele Identifier: CA492204301

Gene: VPS33B

Linked Data

• MyVariant Identifiers: chr15:g.91545338C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002108C>T , CM000677.2:g.91002108C>T	GRCh38
NC_000015.9:g.91545338C>T , CM000677.1:g.91545338C>T	GRCh37
NC_000015.8:g.89346342C>T	NCBI36
NG_012162.1:g.25496G>A , LRG_884:g.25496G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1347G>A MANE Select	ENSP00000327650.4:p.Gly449=
ENST00000643536.1:c.1347G>A	ENSP00000494429.1:p.Gly449=
ENST00000647331.1:c.1347G>A	ENSP00000493953.1:p.Gly449=
ENST00000333371.7:c.1347G>A	ENSP00000327650.3:p.Gly449=
ENST00000535906.1:c.1266G>A	ENSP00000444053.1:p.Gly422=
ENST00000574755.5:c.*1042G>A	ENSP00000460413.1:n.*1042G>A
NM_001289148.1:c.1266G>A	NP_001276077.1:p.Gly422=
NM_001289149.1:c.1074G>A	NP_001276078.1:p.Gly358=
NM_018668.4:c.1347G>A , LRG_884t1:c.1347G>A	NP_061138.3:p.Gly449=
XM_005254884.2:c.1269G>A	XP_005254941.1:p.Gly423=
XM_005254887.1:c.1074G>A	XP_005254944.1:p.Gly358=
XM_011521448.1:c.1074G>A	XP_011519750.1:p.Gly358=
XM_011521449.1:c.1023G>A	XP_011519751.1:p.Gly341=
XM_011521449.2:c.1023G>A	XP_011519751.1:p.Gly341=
XM_017022075.2:c.1002G>A	XP_016877564.1:p.Gly334=
XM_017022076.1:c.1002G>A	XP_016877565.1:p.Gly334=
XR_001751213.2:n.1845G>A
NM_018668.5:c.1347G>A MANE Select	NP_061138.3:p.Gly449=