Canonical Allele Identifier: CA492173218

Gene: VPS33B

Linked Data

• MyVariant Identifiers: chr15:g.91557660C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91014430C>T , CM000677.2:g.91014430C>T	GRCh38
NC_000015.9:g.91557660C>T , CM000677.1:g.91557660C>T	GRCh37
NC_000015.8:g.89358664C>T	NCBI36
NG_012162.1:g.13174G>A , LRG_884:g.13174G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.243G>A MANE Select	ENSP00000327650.4:p.Leu81=
ENST00000643536.1:c.243G>A	ENSP00000494429.1:p.Leu81=
ENST00000647331.1:c.243G>A	ENSP00000493953.1:p.Leu81=
ENST00000333371.7:c.243G>A	ENSP00000327650.3:p.Leu81=
ENST00000535906.1:c.162G>A	ENSP00000444053.1:p.Leu54=
ENST00000554264.5:n.166G>A
ENST00000556096.6:n.637G>A
ENST00000557358.1:n.447G>A
ENST00000574755.5:c.181G>A	ENSP00000460413.1:p.Val61Met
NM_001289148.1:c.162G>A	NP_001276077.1:p.Leu54=
NM_001289149.1:c.-31G>A	NP_001276078.1:n.-31G>A
NM_018668.4:c.243G>A , LRG_884t1:c.243G>A	NP_061138.3:p.Leu81=
XM_005254884.2:c.243G>A	XP_005254941.1:p.Leu81=
XM_005254887.1:c.-31G>A	XP_005254944.1:n.-31G>A
XM_005254888.2:c.243G>A	XP_005254945.1:p.Leu81=
XM_011521448.1:c.-31G>A	XP_011519750.1:n.-31G>A
XM_017022075.2:c.-119G>A	XP_016877564.1:n.-119G>A
XM_017022076.1:c.-119G>A	XP_016877565.1:n.-119G>A
XR_001751213.2:n.579G>A
NM_018668.5:c.243G>A MANE Select	NP_061138.3:p.Leu81=