Canonical Allele Identifier: CA397488559

Gene: VPS53

Linked Data

• MyVariant Identifiers: chr17:g.465744T>A (hg19) ; chr17:g.562504T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.562504T>A , CM000679.2:g.562504T>A	GRCh38
NC_000017.10:g.465744T>A , CM000679.1:g.465744T>A	GRCh37
NC_000017.9:g.412494T>A	NCBI36
NG_034190.1:g.157353A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000291074.10:c.1468A>T	ENSP00000291074.5:p.Lys490Ter
ENST00000437048.7:c.1555A>T MANE Select	ENSP00000401435.2:p.Lys519Ter
ENST00000571805.6:c.1555A>T	ENSP00000459312.1:p.Lys519Ter
ENST00000572334.7:c.1186A>T	ENSP00000506188.1:p.Lys396Ter
ENST00000572607.2:n.385A>T
ENST00000679361.1:c.1555A>T	ENSP00000504978.1:p.Lys519Ter
ENST00000679959.1:c.1088A>T	ENSP00000506180.1:n.1088A>T
ENST00000680069.1:c.1555A>T	ENSP00000505145.1:p.Lys519Ter
ENST00000680114.1:c.1081A>T	ENSP00000505327.1:p.Lys361Ter
ENST00000680128.1:c.1351A>T	ENSP00000506159.1:p.Lys451Ter
ENST00000680274.1:n.1117A>T
ENST00000680465.1:c.1555A>T	ENSP00000505997.1:p.Lys519Ter
ENST00000680641.1:c.*1375A>T	ENSP00000505237.1:n.*1375A>T
ENST00000680702.1:n.460A>T
ENST00000680704.1:c.1186A>T	ENSP00000506453.1:p.Lys396Ter
ENST00000680872.1:c.*681A>T	ENSP00000506605.1:n.*681A>T
ENST00000680944.1:n.950A>T
ENST00000680958.1:n.1462A>T
ENST00000681096.1:c.1096A>T	ENSP00000506052.1:p.Lys366Ter
ENST00000681154.1:c.1468A>T	ENSP00000505866.1:p.Lys490Ter
ENST00000681160.1:c.1186A>T	ENSP00000504905.1:p.Lys396Ter
ENST00000681317.1:c.1555A>T	ENSP00000505190.1:p.Lys519Ter
ENST00000681478.1:c.*1375A>T	ENSP00000505041.1:n.*1375A>T
ENST00000681510.1:c.1405A>T	ENSP00000505594.1:p.Lys469Ter
ENST00000681600.1:n.650A>T
ENST00000681661.1:c.*536A>T	ENSP00000506596.1:n.*536A>T
ENST00000681830.1:c.1104A>T	ENSP00000505322.1:n.1104A>T
ENST00000681897.1:n.807A>T
ENST00000681902.1:c.1555A>T	ENSP00000505328.1:p.Lys519Ter
ENST00000681917.1:c.1024A>T	ENSP00000505944.1:p.Lys342Ter
ENST00000681943.1:c.1421A>T	ENSP00000504889.1:n.1421A>T
ENST00000681946.1:c.*536A>T	ENSP00000505563.1:n.*536A>T
ENST00000291074.9:c.1468A>T	ENSP00000291074.5:p.Lys490Ter
ENST00000389040.9:c.1411A>T	ENSP00000373692.5:p.Lys471Ter
ENST00000401468.7:c.724A>T	ENSP00000384294.3:p.Lys242Ter
ENST00000437048.6:c.1555A>T	ENSP00000401435.2:p.Lys519Ter
ENST00000571805.5:c.1555A>T	ENSP00000459312.1:p.Lys519Ter
ENST00000572607.1:n.183A>T
ENST00000573028.5:c.*1002A>T	ENSP00000458311.1:n.*1002A>T
ENST00000574029.5:c.207-44865A>T	ENSP00000459159.1:n.207-44865A>T
ENST00000576149.5:n.1325A>T
NM_001128159.2:c.1555A>T	NP_001121631.1:p.Lys519Ter
NM_018289.3:c.1468A>T	NP_060759.2:p.Lys490Ter
XM_011523953.1:c.961A>T	XP_011522255.1:p.Lys321Ter
XR_934061.1:n.1852A>T
XR_934062.1:n.1607A>T
NM_001366253.1:c.1555A>T	NP_001353182.1:p.Lys519Ter
NM_001366254.1:c.961A>T	NP_001353183.1:p.Lys321Ter
XM_017024817.2:c.1405A>T	XP_016880306.1:p.Lys469Ter
XM_017024818.1:c.1186A>T	XP_016880307.1:p.Lys396Ter
XR_001752553.2:n.1692A>T
XR_934061.3:n.1842A>T
XR_934062.2:n.1597A>T
NM_001128159.3:c.1555A>T MANE Select	NP_001121631.1:p.Lys519Ter
NM_001366253.2:c.1555A>T	NP_001353182.1:p.Lys519Ter
NM_001366254.2:c.961A>T	NP_001353183.1:p.Lys321Ter
NM_018289.4:c.1468A>T	NP_060759.2:p.Lys490Ter