Canonical Allele Identifier: CA2635138821

Gene: VPS53

Linked Data

• gnomAD v4: 17-532822-TGATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.532823_532826del , CM000679.2:g.532823_532826del	GRCh38
NC_000017.10:g.436063_436066del , CM000679.1:g.436063_436066del	GRCh37
NC_000017.9:g.382813_382816del	NCBI36
NG_034190.1:g.187031_187034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291074.10:c.*1_*4del	ENSP00000291074.5:n.*1_*4del
ENST00000437048.7:c.2085+16_2085+19del MANE Select	ENSP00000401435.2:n.2085+16_2085+19del
ENST00000571805.6:c.*1_*4del	ENSP00000459312.1:n.*1_*4del
ENST00000679817.1:c.*1_*4del	ENSP00000505032.1:n.*1_*4del
ENST00000680128.1:c.*1_*4del	ENSP00000506159.1:n.*1_*4del
ENST00000680465.1:c.2085+16_2085+19del	ENSP00000505997.1:n.2085+16_2085+19del
ENST00000680641.1:c.*3334+16_*3334+19del	ENSP00000505237.1:n.*3334+16_*3334+19del
ENST00000680872.1:c.*1211+16_*1211+19del	ENSP00000506605.1:n.*1211+16_*1211+19del
ENST00000681050.1:c.298+16_298+19del
ENST00000681096.1:c.*1_*4del	ENSP00000506052.1:n.*1_*4del
ENST00000681103.1:c.315+16_315+19del	ENSP00000505892.1:n.315+16_315+19del
ENST00000681160.1:c.1716+16_1716+19del	ENSP00000504905.1:n.1716+16_1716+19del
ENST00000681317.1:c.2015+4202_2015+4205del	ENSP00000505190.1:n.2015+4202_2015+4205del
ENST00000681478.1:c.*1921_*1924del	ENSP00000505041.1:n.*1921_*1924del
ENST00000681510.1:c.1935+16_1935+19del	ENSP00000505594.1:n.1935+16_1935+19del
ENST00000681600.1:n.1180+16_1180+19del
ENST00000681661.1:c.*1066+16_*1066+19del	ENSP00000506596.1:n.*1066+16_*1066+19del
ENST00000681858.1:c.315+16_315+19del	ENSP00000505044.1:n.315+16_315+19del
ENST00000681917.1:c.1554+16_1554+19del	ENSP00000505944.1:n.1554+16_1554+19del
ENST00000681943.1:c.1803+16_1803+19del	ENSP00000504889.1:n.1803+16_1803+19del
ENST00000681946.1:c.*1066+16_*1066+19del	ENSP00000505563.1:n.*1066+16_*1066+19del
ENST00000291074.9:c.*1_*4del	ENSP00000291074.5:n.*1_*4del
ENST00000437048.6:c.2085+16_2085+19del	ENSP00000401435.2:n.2085+16_2085+19del
ENST00000570771.1:n.152+16_152+19del
ENST00000571805.5:c.*1_*4del	ENSP00000459312.1:n.*1_*4del
ENST00000573028.5:c.*1548_*1551del	ENSP00000458311.1:n.*1548_*1551del
ENST00000574029.5:c.207-15187_207-15184del	ENSP00000459159.1:n.207-15187_207-15184del
ENST00000576149.5:n.1855+16_1855+19del
NM_001128159.2:c.2085+16_2085+19del	NP_001121631.1:n.2085+16_2085+19del
NM_018289.3:c.*1_*4del	NP_060759.2:n.*1_*4del
XM_011523953.1:c.*1_*4del	XP_011522255.1:n.*1_*4del
XR_934061.1:n.2382+16_2382+19del
XR_934133.1:n.291-7566_291-7563del
NM_001366253.1:c.*1_*4del	NP_001353182.1:n.*1_*4del
NM_001366254.1:c.*1_*4del	NP_001353183.1:n.*1_*4del
XM_017024817.2:c.1935+16_1935+19del	XP_016880306.1:n.1935+16_1935+19del
XM_017024818.1:c.1716+16_1716+19del	XP_016880307.1:n.1716+16_1716+19del
XR_001752553.2:n.2222+16_2222+19del
XR_934061.3:n.2372+16_2372+19del
NM_001128159.3:c.2085+16_2085+19del MANE Select	NP_001121631.1:n.2085+16_2085+19del
NM_001366253.2:c.*1_*4del	NP_001353182.1:n.*1_*4del
NM_001366254.2:c.*1_*4del	NP_001353183.1:n.*1_*4del
NM_018289.4:c.*1_*4del	NP_060759.2:n.*1_*4del