Canonical Allele Identifier: CA2635138520

Gene: VPS53

Linked Data

• gnomAD v4: 17-532692-TAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532695_532697del , CM000679.2:g.532695_532697del	GRCh38
NC_000017.10:g.435935_435937del , CM000679.1:g.435935_435937del	GRCh37
NC_000017.9:g.382685_382687del	NCBI36
NG_034190.1:g.187162_187164del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.*132_*134del	ENSP00000291074.5:n.*132_*134del
ENST00000437048.7:c.2085+147_2085+149del MANE Select	ENSP00000401435.2:n.2085+147_2085+149del
ENST00000571805.6:c.*132_*134del	ENSP00000459312.1:n.*132_*134del
ENST00000680128.1:c.*132_*134del	ENSP00000506159.1:n.*132_*134del
ENST00000680465.1:c.2085+147_2085+149del	ENSP00000505997.1:n.2085+147_2085+149del
ENST00000680641.1:c.*3334+147_*3334+149del	ENSP00000505237.1:n.*3334+147_*3334+149del
ENST00000680872.1:c.*1211+147_*1211+149del	ENSP00000506605.1:n.*1211+147_*1211+149del
ENST00000681050.1:c.298+147_298+149del
ENST00000681096.1:c.*132_*134del	ENSP00000506052.1:n.*132_*134del
ENST00000681103.1:c.315+147_315+149del	ENSP00000505892.1:n.315+147_315+149del
ENST00000681160.1:c.1716+147_1716+149del	ENSP00000504905.1:n.1716+147_1716+149del
ENST00000681317.1:c.2015+4333_2015+4335del	ENSP00000505190.1:n.2015+4333_2015+4335del
ENST00000681478.1:c.*2052_*2054del	ENSP00000505041.1:n.*2052_*2054del
ENST00000681510.1:c.1935+147_1935+149del	ENSP00000505594.1:n.1935+147_1935+149del
ENST00000681600.1:n.1180+147_1180+149del
ENST00000681661.1:c.*1066+147_*1066+149del	ENSP00000506596.1:n.*1066+147_*1066+149del
ENST00000681858.1:c.315+147_315+149del	ENSP00000505044.1:n.315+147_315+149del
ENST00000681917.1:c.1554+147_1554+149del	ENSP00000505944.1:n.1554+147_1554+149del
ENST00000681943.1:c.1803+147_1803+149del	ENSP00000504889.1:n.1803+147_1803+149del
ENST00000681946.1:c.*1066+147_*1066+149del	ENSP00000505563.1:n.*1066+147_*1066+149del
ENST00000291074.9:c.*132_*134del	ENSP00000291074.5:n.*132_*134del
ENST00000437048.6:c.2085+147_2085+149del	ENSP00000401435.2:n.2085+147_2085+149del
ENST00000570771.1:n.152+147_152+149del
ENST00000573028.5:c.*1679_*1681del	ENSP00000458311.1:n.*1679_*1681del
ENST00000574029.5:c.207-15056_207-15054del	ENSP00000459159.1:n.207-15056_207-15054del
ENST00000576149.5:n.1855+147_1855+149del
NM_001128159.2:c.2085+147_2085+149del	NP_001121631.1:n.2085+147_2085+149del
NM_018289.3:c.*132_*134del	NP_060759.2:n.*132_*134del
XR_934061.1:n.2382+147_2382+149del
XR_934133.1:n.291-7694_291-7692del
XM_017024817.2:c.1935+147_1935+149del	XP_016880306.1:n.1935+147_1935+149del
XM_017024818.1:c.1716+147_1716+149del	XP_016880307.1:n.1716+147_1716+149del
XR_001752553.2:n.2222+147_2222+149del
XR_934061.3:n.2372+147_2372+149del
NM_001128159.3:c.2085+147_2085+149del MANE Select	NP_001121631.1:n.2085+147_2085+149del
NM_001366253.2:c.*132_*134del	NP_001353182.1:n.*132_*134del
NM_001366254.2:c.*132_*134del	NP_001353183.1:n.*132_*134del
NM_018289.4:c.*132_*134del	NP_060759.2:n.*132_*134del