Canonical Allele Identifier: CA8261193

Gene: VPS53

Linked Data

• ClinVar Variation Id: 2955763
• ClinVar RCV Id: RCV003810914
• dbSNP Id: rs141390855
• ExAC: 17:436071 G / A
• gnomAD v2: 17-436071-G-A
• gnomAD v3: 17-532831-G-A
• gnomAD v4: 17-532831-G-A
• MyVariant Identifiers: chr17:g.436071G>A (hg19) ; chr17:g.532831G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532831G>A , CM000679.2:g.532831G>A	GRCh38
NC_000017.10:g.436071G>A , CM000679.1:g.436071G>A	GRCh37
NC_000017.9:g.382821G>A	NCBI36
NG_034190.1:g.187026C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.2009C>T	ENSP00000291074.5:p.Thr670Met
ENST00000437048.7:c.2085+11C>T MANE Select	ENSP00000401435.2:n.2085+11C>T
ENST00000571805.6:c.2096C>T	ENSP00000459312.1:p.Thr699Met
ENST00000679817.1:c.326C>T	ENSP00000505032.1:p.Thr109Met
ENST00000680128.1:c.1892C>T	ENSP00000506159.1:p.Thr631Met
ENST00000680465.1:c.2085+11C>T	ENSP00000505997.1:n.2085+11C>T
ENST00000680641.1:c.*3334+11C>T	ENSP00000505237.1:n.*3334+11C>T
ENST00000680872.1:c.*1211+11C>T	ENSP00000506605.1:n.*1211+11C>T
ENST00000681050.1:c.298+11C>T
ENST00000681096.1:c.1637C>T	ENSP00000506052.1:p.Thr546Met
ENST00000681103.1:c.315+11C>T	ENSP00000505892.1:n.315+11C>T
ENST00000681160.1:c.1716+11C>T	ENSP00000504905.1:n.1716+11C>T
ENST00000681317.1:c.2015+4197C>T	ENSP00000505190.1:n.2015+4197C>T
ENST00000681478.1:c.*1916C>T	ENSP00000505041.1:n.*1916C>T
ENST00000681510.1:c.1935+11C>T	ENSP00000505594.1:n.1935+11C>T
ENST00000681600.1:n.1180+11C>T
ENST00000681661.1:c.*1066+11C>T	ENSP00000506596.1:n.*1066+11C>T
ENST00000681858.1:c.315+11C>T	ENSP00000505044.1:n.315+11C>T
ENST00000681917.1:c.1554+11C>T	ENSP00000505944.1:n.1554+11C>T
ENST00000681943.1:c.1803+11C>T	ENSP00000504889.1:n.1803+11C>T
ENST00000681946.1:c.*1066+11C>T	ENSP00000505563.1:n.*1066+11C>T
ENST00000291074.9:c.2009C>T	ENSP00000291074.5:p.Thr670Met
ENST00000389040.9:c.1899C>T	ENSP00000373692.5:n.1899C>T
ENST00000401468.7:c.1265C>T	ENSP00000384294.3:p.Thr422Met
ENST00000437048.6:c.2085+11C>T	ENSP00000401435.2:n.2085+11C>T
ENST00000570771.1:n.152+11C>T
ENST00000571805.5:c.2096C>T	ENSP00000459312.1:p.Thr699Met
ENST00000573028.5:c.*1543C>T	ENSP00000458311.1:n.*1543C>T
ENST00000574029.5:c.207-15192C>T	ENSP00000459159.1:n.207-15192C>T
ENST00000576149.5:n.1855+11C>T
NM_001128159.2:c.2085+11C>T	NP_001121631.1:n.2085+11C>T
NM_018289.3:c.2009C>T	NP_060759.2:p.Thr670Met
XM_011523953.1:c.1502C>T	XP_011522255.1:p.Thr501Met
XR_934061.1:n.2382+11C>T
XR_934133.1:n.291-7558G>A
NM_001366253.1:c.2096C>T	NP_001353182.1:p.Thr699Met
NM_001366254.1:c.1502C>T	NP_001353183.1:p.Thr501Met
XM_017024817.2:c.1935+11C>T	XP_016880306.1:n.1935+11C>T
XM_017024818.1:c.1716+11C>T	XP_016880307.1:n.1716+11C>T
XR_001752553.2:n.2222+11C>T
XR_934061.3:n.2372+11C>T
NM_001128159.3:c.2085+11C>T MANE Select	NP_001121631.1:n.2085+11C>T
NM_001366253.2:c.2096C>T	NP_001353182.1:p.Thr699Met
NM_001366254.2:c.1502C>T	NP_001353183.1:p.Thr501Met
NM_018289.4:c.2009C>T	NP_060759.2:p.Thr670Met