Canonical Allele Identifier: CA397710474

Gene: VPS53

Linked Data

• MyVariant Identifiers: chr17:g.436147A>T (hg19) ; chr17:g.532907A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532907A>T , CM000679.2:g.532907A>T	GRCh38
NC_000017.10:g.436147A>T , CM000679.1:g.436147A>T	GRCh37
NC_000017.9:g.382897A>T	NCBI36
NG_034190.1:g.186950T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.1933T>A	ENSP00000291074.5:p.Phe645Ile
ENST00000437048.7:c.2020T>A MANE Select	ENSP00000401435.2:p.Phe674Ile
ENST00000571805.6:c.2020T>A	ENSP00000459312.1:p.Phe674Ile
ENST00000572334.7:c.1651T>A	ENSP00000506188.1:p.Phe551Ile
ENST00000679817.1:c.250T>A	ENSP00000505032.1:p.Phe84Ile
ENST00000680128.1:c.1816T>A	ENSP00000506159.1:p.Phe606Ile
ENST00000680465.1:c.2020T>A	ENSP00000505997.1:p.Phe674Ile
ENST00000680641.1:c.*3269T>A	ENSP00000505237.1:n.*3269T>A
ENST00000680704.1:c.1651T>A	ENSP00000506453.1:p.Phe551Ile
ENST00000680872.1:c.*1146T>A	ENSP00000506605.1:n.*1146T>A
ENST00000681050.1:c.233T>A
ENST00000681096.1:c.1561T>A	ENSP00000506052.1:p.Phe521Ile
ENST00000681103.1:c.250T>A	ENSP00000505892.1:p.Phe84Ile
ENST00000681160.1:c.1651T>A	ENSP00000504905.1:p.Phe551Ile
ENST00000681317.1:c.2015+4121T>A	ENSP00000505190.1:n.2015+4121T>A
ENST00000681478.1:c.*1840T>A	ENSP00000505041.1:n.*1840T>A
ENST00000681510.1:c.1870T>A	ENSP00000505594.1:p.Phe624Ile
ENST00000681600.1:n.1115T>A
ENST00000681661.1:c.*1001T>A	ENSP00000506596.1:n.*1001T>A
ENST00000681858.1:c.250T>A	ENSP00000505044.1:p.Phe84Ile
ENST00000681917.1:c.1489T>A	ENSP00000505944.1:p.Phe497Ile
ENST00000681943.1:c.1738T>A	ENSP00000504889.1:n.1738T>A
ENST00000681946.1:c.*1001T>A	ENSP00000505563.1:n.*1001T>A
ENST00000291074.9:c.1933T>A	ENSP00000291074.5:p.Phe645Ile
ENST00000389040.9:c.1823T>A	ENSP00000373692.5:n.1823T>A
ENST00000401468.7:c.1189T>A	ENSP00000384294.3:p.Phe397Ile
ENST00000437048.6:c.2020T>A	ENSP00000401435.2:p.Phe674Ile
ENST00000570771.1:n.87T>A
ENST00000571805.5:c.2020T>A	ENSP00000459312.1:p.Phe674Ile
ENST00000573028.5:c.*1467T>A	ENSP00000458311.1:n.*1467T>A
ENST00000574029.5:c.207-15268T>A	ENSP00000459159.1:n.207-15268T>A
ENST00000576149.5:n.1790T>A
NM_001128159.2:c.2020T>A	NP_001121631.1:p.Phe674Ile
NM_018289.3:c.1933T>A	NP_060759.2:p.Phe645Ile
XM_011523953.1:c.1426T>A	XP_011522255.1:p.Phe476Ile
XR_934061.1:n.2317T>A
XR_934133.1:n.291-7482A>T
NM_001366253.1:c.2020T>A	NP_001353182.1:p.Phe674Ile
NM_001366254.1:c.1426T>A	NP_001353183.1:p.Phe476Ile
XM_017024817.2:c.1870T>A	XP_016880306.1:p.Phe624Ile
XM_017024818.1:c.1651T>A	XP_016880307.1:p.Phe551Ile
XR_001752553.2:n.2157T>A
XR_934061.3:n.2307T>A
NM_001128159.3:c.2020T>A MANE Select	NP_001121631.1:p.Phe674Ile
NM_001366253.2:c.2020T>A	NP_001353182.1:p.Phe674Ile
NM_001366254.2:c.1426T>A	NP_001353183.1:p.Phe476Ile
NM_018289.4:c.1933T>A	NP_060759.2:p.Phe645Ile