Canonical Allele Identifier: CA2635139018

Gene: VPS53

Linked Data

• gnomAD v4: 17-532939-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532939A>G , CM000679.2:g.532939A>G	GRCh38
NC_000017.10:g.436179A>G , CM000679.1:g.436179A>G	GRCh37
NC_000017.9:g.382929A>G	NCBI36
NG_034190.1:g.186918T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.1929-28T>C	ENSP00000291074.5:n.1929-28T>C
ENST00000437048.7:c.2016-28T>C MANE Select	ENSP00000401435.2:n.2016-28T>C
ENST00000571805.6:c.2016-28T>C	ENSP00000459312.1:n.2016-28T>C
ENST00000572334.7:c.1647-28T>C	ENSP00000506188.1:n.1647-28T>C
ENST00000679817.1:c.246-28T>C	ENSP00000505032.1:n.246-28T>C
ENST00000680128.1:c.1812-28T>C	ENSP00000506159.1:n.1812-28T>C
ENST00000680465.1:c.2016-28T>C	ENSP00000505997.1:n.2016-28T>C
ENST00000680641.1:c.*3265-28T>C	ENSP00000505237.1:n.*3265-28T>C
ENST00000680704.1:c.1647-28T>C	ENSP00000506453.1:n.1647-28T>C
ENST00000680872.1:c.*1142-28T>C	ENSP00000506605.1:n.*1142-28T>C
ENST00000681050.1:c.229-28T>C
ENST00000681096.1:c.1557-28T>C	ENSP00000506052.1:n.1557-28T>C
ENST00000681103.1:c.246-28T>C	ENSP00000505892.1:n.246-28T>C
ENST00000681160.1:c.1647-28T>C	ENSP00000504905.1:n.1647-28T>C
ENST00000681317.1:c.2015+4089T>C	ENSP00000505190.1:n.2015+4089T>C
ENST00000681478.1:c.*1836-28T>C	ENSP00000505041.1:n.*1836-28T>C
ENST00000681510.1:c.1866-28T>C	ENSP00000505594.1:n.1866-28T>C
ENST00000681600.1:n.1111-28T>C
ENST00000681661.1:c.*997-28T>C	ENSP00000506596.1:n.*997-28T>C
ENST00000681858.1:c.246-28T>C	ENSP00000505044.1:n.246-28T>C
ENST00000681917.1:c.1485-28T>C	ENSP00000505944.1:n.1485-28T>C
ENST00000681943.1:c.1734-28T>C	ENSP00000504889.1:n.1734-28T>C
ENST00000681946.1:c.*997-28T>C	ENSP00000505563.1:n.*997-28T>C
ENST00000291074.9:c.1929-28T>C	ENSP00000291074.5:n.1929-28T>C
ENST00000389040.9:c.1819-28T>C	ENSP00000373692.5:n.1819-28T>C
ENST00000401468.7:c.1185-28T>C	ENSP00000384294.3:n.1185-28T>C
ENST00000437048.6:c.2016-28T>C	ENSP00000401435.2:n.2016-28T>C
ENST00000570771.1:n.55T>C
ENST00000571805.5:c.2016-28T>C	ENSP00000459312.1:n.2016-28T>C
ENST00000573028.5:c.*1463-28T>C	ENSP00000458311.1:n.*1463-28T>C
ENST00000574029.5:c.207-15300T>C	ENSP00000459159.1:n.207-15300T>C
ENST00000576149.5:n.1786-28T>C
NM_001128159.2:c.2016-28T>C	NP_001121631.1:n.2016-28T>C
NM_018289.3:c.1929-28T>C	NP_060759.2:n.1929-28T>C
XM_011523953.1:c.1422-28T>C	XP_011522255.1:n.1422-28T>C
XR_934061.1:n.2313-28T>C
XR_934133.1:n.291-7450A>G
NM_001366253.1:c.2016-28T>C	NP_001353182.1:n.2016-28T>C
NM_001366254.1:c.1422-28T>C	NP_001353183.1:n.1422-28T>C
XM_017024817.2:c.1866-28T>C	XP_016880306.1:n.1866-28T>C
XM_017024818.1:c.1647-28T>C	XP_016880307.1:n.1647-28T>C
XR_001752553.2:n.2153-28T>C
XR_934061.3:n.2303-28T>C
NM_001128159.3:c.2016-28T>C MANE Select	NP_001121631.1:n.2016-28T>C
NM_001366253.2:c.2016-28T>C	NP_001353182.1:n.2016-28T>C
NM_001366254.2:c.1422-28T>C	NP_001353183.1:n.1422-28T>C
NM_018289.4:c.1929-28T>C	NP_060759.2:n.1929-28T>C