Canonical Allele Identifier: CA2242366270

Gene: VPS53

Linked Data

• dbSNP Id: rs1909690171

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532736_532738del , CM000679.2:g.532736_532738del	GRCh38
NC_000017.10:g.435976_435978del , CM000679.1:g.435976_435978del	GRCh37
NC_000017.9:g.382726_382728del	NCBI36
NG_034190.1:g.187119_187121del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.*89_*91del	ENSP00000291074.5:n.*89_*91del
ENST00000437048.7:c.2085+104_2085+106del MANE Select	ENSP00000401435.2:n.2085+104_2085+106del
ENST00000571805.6:c.*89_*91del	ENSP00000459312.1:n.*89_*91del
ENST00000679817.1:c.*89_*91del	ENSP00000505032.1:n.*89_*91del
ENST00000680128.1:c.*89_*91del	ENSP00000506159.1:n.*89_*91del
ENST00000680465.1:c.2085+104_2085+106del	ENSP00000505997.1:n.2085+104_2085+106del
ENST00000680641.1:c.*3334+104_*3334+106del	ENSP00000505237.1:n.*3334+104_*3334+106del
ENST00000680872.1:c.*1211+104_*1211+106del	ENSP00000506605.1:n.*1211+104_*1211+106del
ENST00000681050.1:c.298+104_298+106del
ENST00000681096.1:c.*89_*91del	ENSP00000506052.1:n.*89_*91del
ENST00000681103.1:c.315+104_315+106del	ENSP00000505892.1:n.315+104_315+106del
ENST00000681160.1:c.1716+104_1716+106del	ENSP00000504905.1:n.1716+104_1716+106del
ENST00000681317.1:c.2015+4290_2015+4292del	ENSP00000505190.1:n.2015+4290_2015+4292del
ENST00000681478.1:c.*2009_*2011del	ENSP00000505041.1:n.*2009_*2011del
ENST00000681510.1:c.1935+104_1935+106del	ENSP00000505594.1:n.1935+104_1935+106del
ENST00000681600.1:n.1180+104_1180+106del
ENST00000681661.1:c.*1066+104_*1066+106del	ENSP00000506596.1:n.*1066+104_*1066+106del
ENST00000681858.1:c.315+104_315+106del	ENSP00000505044.1:n.315+104_315+106del
ENST00000681917.1:c.1554+104_1554+106del	ENSP00000505944.1:n.1554+104_1554+106del
ENST00000681943.1:c.1803+104_1803+106del	ENSP00000504889.1:n.1803+104_1803+106del
ENST00000681946.1:c.*1066+104_*1066+106del	ENSP00000505563.1:n.*1066+104_*1066+106del
ENST00000291074.9:c.*89_*91del	ENSP00000291074.5:n.*89_*91del
ENST00000437048.6:c.2085+104_2085+106del	ENSP00000401435.2:n.2085+104_2085+106del
ENST00000570771.1:n.152+104_152+106del
ENST00000571805.5:c.*89_*91del	ENSP00000459312.1:n.*89_*91del
ENST00000573028.5:c.*1636_*1638del	ENSP00000458311.1:n.*1636_*1638del
ENST00000574029.5:c.207-15099_207-15097del	ENSP00000459159.1:n.207-15099_207-15097del
ENST00000576149.5:n.1855+104_1855+106del
NM_001128159.2:c.2085+104_2085+106del	NP_001121631.1:n.2085+104_2085+106del
NM_018289.3:c.*89_*91del	NP_060759.2:n.*89_*91del
XM_011523953.1:c.*89_*91del	XP_011522255.1:n.*89_*91del
XR_934061.1:n.2382+104_2382+106del
XR_934133.1:n.291-7653_291-7651del
NM_001366253.1:c.*89_*91del	NP_001353182.1:n.*89_*91del
NM_001366254.1:c.*89_*91del	NP_001353183.1:n.*89_*91del
XM_017024817.2:c.1935+104_1935+106del	XP_016880306.1:n.1935+104_1935+106del
XM_017024818.1:c.1716+104_1716+106del	XP_016880307.1:n.1716+104_1716+106del
XR_001752553.2:n.2222+104_2222+106del
XR_934061.3:n.2372+104_2372+106del
NM_001128159.3:c.2085+104_2085+106del MANE Select	NP_001121631.1:n.2085+104_2085+106del
NM_001366253.2:c.*89_*91del	NP_001353182.1:n.*89_*91del
NM_001366254.2:c.*89_*91del	NP_001353183.1:n.*89_*91del
NM_018289.4:c.*89_*91del	NP_060759.2:n.*89_*91del