Canonical Allele Identifier: CA393886698

Gene: VPS33B

Linked Data

• MyVariant Identifiers: chr15:g.91545385A>C (hg19) ; chr15:g.91002155A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002155A>C , CM000677.2:g.91002155A>C	GRCh38
NC_000015.9:g.91545385A>C , CM000677.1:g.91545385A>C	GRCh37
NC_000015.8:g.89346389A>C	NCBI36
NG_012162.1:g.25449T>G , LRG_884:g.25449T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1300T>G MANE Select	ENSP00000327650.4:p.Phe434Val
ENST00000643536.1:c.1300T>G	ENSP00000494429.1:p.Phe434Val
ENST00000647331.1:c.1300T>G	ENSP00000493953.1:p.Phe434Val
ENST00000333371.7:c.1300T>G	ENSP00000327650.3:p.Phe434Val
ENST00000535906.1:c.1219T>G	ENSP00000444053.1:p.Phe407Val
ENST00000574755.5:c.*995T>G	ENSP00000460413.1:n.*995T>G
NM_001289148.1:c.1219T>G	NP_001276077.1:p.Phe407Val
NM_001289149.1:c.1027T>G	NP_001276078.1:p.Phe343Val
NM_018668.4:c.1300T>G , LRG_884t1:c.1300T>G	NP_061138.3:p.Phe434Val
XM_005254884.2:c.1222T>G	XP_005254941.1:p.Phe408Val
XM_005254887.1:c.1027T>G	XP_005254944.1:p.Phe343Val
XM_011521448.1:c.1027T>G	XP_011519750.1:p.Phe343Val
XM_011521449.1:c.976T>G	XP_011519751.1:p.Phe326Val
XM_011521449.2:c.976T>G	XP_011519751.1:p.Phe326Val
XM_017022075.2:c.955T>G	XP_016877564.1:p.Phe319Val
XM_017022076.1:c.955T>G	XP_016877565.1:p.Phe319Val
XR_001751213.2:n.1798T>G
NM_018668.5:c.1300T>G MANE Select	NP_061138.3:p.Phe434Val