Canonical Allele Identifier: CA397710231

Gene: VPS53

Linked Data

• MyVariant Identifiers: chr17:g.436089G>A (hg19) ; chr17:g.532849G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532849G>A , CM000679.2:g.532849G>A	GRCh38
NC_000017.10:g.436089G>A , CM000679.1:g.436089G>A	GRCh37
NC_000017.9:g.382839G>A	NCBI36
NG_034190.1:g.187008C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.1991C>T	ENSP00000291074.5:p.Ala664Val
ENST00000437048.7:c.2078C>T MANE Select	ENSP00000401435.2:p.Ala693Val
ENST00000571805.6:c.2078C>T	ENSP00000459312.1:p.Ala693Val
ENST00000572334.7:c.1709C>T	ENSP00000506188.1:p.Ala570Val
ENST00000679817.1:c.308C>T	ENSP00000505032.1:p.Ala103Val
ENST00000680128.1:c.1874C>T	ENSP00000506159.1:p.Ala625Val
ENST00000680465.1:c.2078C>T	ENSP00000505997.1:p.Ala693Val
ENST00000680641.1:c.*3327C>T	ENSP00000505237.1:n.*3327C>T
ENST00000680704.1:c.1709C>T	ENSP00000506453.1:p.Ala570Val
ENST00000680872.1:c.*1204C>T	ENSP00000506605.1:n.*1204C>T
ENST00000681050.1:c.291C>T
ENST00000681096.1:c.1619C>T	ENSP00000506052.1:p.Ala540Val
ENST00000681103.1:c.308C>T	ENSP00000505892.1:p.Ala103Val
ENST00000681160.1:c.1709C>T	ENSP00000504905.1:p.Ala570Val
ENST00000681317.1:c.2015+4179C>T	ENSP00000505190.1:n.2015+4179C>T
ENST00000681478.1:c.*1898C>T	ENSP00000505041.1:n.*1898C>T
ENST00000681510.1:c.1928C>T	ENSP00000505594.1:p.Ala643Val
ENST00000681600.1:n.1173C>T
ENST00000681661.1:c.*1059C>T	ENSP00000506596.1:n.*1059C>T
ENST00000681858.1:c.308C>T	ENSP00000505044.1:p.Ala103Val
ENST00000681917.1:c.1547C>T	ENSP00000505944.1:p.Ala516Val
ENST00000681943.1:c.1796C>T	ENSP00000504889.1:n.1796C>T
ENST00000681946.1:c.*1059C>T	ENSP00000505563.1:n.*1059C>T
ENST00000291074.9:c.1991C>T	ENSP00000291074.5:p.Ala664Val
ENST00000389040.9:c.1881C>T	ENSP00000373692.5:n.1881C>T
ENST00000401468.7:c.1247C>T	ENSP00000384294.3:p.Ala416Val
ENST00000437048.6:c.2078C>T	ENSP00000401435.2:p.Ala693Val
ENST00000570771.1:n.145C>T
ENST00000571805.5:c.2078C>T	ENSP00000459312.1:p.Ala693Val
ENST00000573028.5:c.*1525C>T	ENSP00000458311.1:n.*1525C>T
ENST00000574029.5:c.207-15210C>T	ENSP00000459159.1:n.207-15210C>T
ENST00000576149.5:n.1848C>T
NM_001128159.2:c.2078C>T	NP_001121631.1:p.Ala693Val
NM_018289.3:c.1991C>T	NP_060759.2:p.Ala664Val
XM_011523953.1:c.1484C>T	XP_011522255.1:p.Ala495Val
XR_934061.1:n.2375C>T
XR_934133.1:n.291-7540G>A
NM_001366253.1:c.2078C>T	NP_001353182.1:p.Ala693Val
NM_001366254.1:c.1484C>T	NP_001353183.1:p.Ala495Val
XM_017024817.2:c.1928C>T	XP_016880306.1:p.Ala643Val
XM_017024818.1:c.1709C>T	XP_016880307.1:p.Ala570Val
XR_001752553.2:n.2215C>T
XR_934061.3:n.2365C>T
NM_001128159.3:c.2078C>T MANE Select	NP_001121631.1:p.Ala693Val
NM_001366253.2:c.2078C>T	NP_001353182.1:p.Ala693Val
NM_001366254.2:c.1484C>T	NP_001353183.1:p.Ala495Val
NM_018289.4:c.1991C>T	NP_060759.2:p.Ala664Val