Canonical Allele Identifier: CA2242382273
Gene: VPS53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.562472C= , CM000679.2:g.562472C= GRCh38
NC_000017.10:g.465712C= , CM000679.1:g.465712C= GRCh37
NC_000017.9:g.412462C= NCBI36
NG_034190.1:g.157385G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291074.10:c.1469+31G= ENSP00000291074.5:n.1469+31G=
ENST00000437048.7:c.1556+31G= MANE Select ENSP00000401435.2:n.1556+31G=
ENST00000571805.6:c.1556+31G= ENSP00000459312.1:n.1556+31G=
ENST00000572334.7:c.1187+31G= ENSP00000506188.1:n.1187+31G=
ENST00000572607.2:n.386+31G=
ENST00000679361.1:c.1556+31G= ENSP00000504978.1:n.1556+31G=
ENST00000679959.1:c.1089+31G= ENSP00000506180.1:n.1089+31G=
ENST00000680069.1:c.1556+31G= ENSP00000505145.1:n.1556+31G=
ENST00000680114.1:c.1082+31G= ENSP00000505327.1:n.1082+31G=
ENST00000680128.1:c.1352+31G= ENSP00000506159.1:n.1352+31G=
ENST00000680274.1:n.1118+31G=
ENST00000680465.1:c.1556+31G= ENSP00000505997.1:n.1556+31G=
ENST00000680641.1:c.*1376+31G= ENSP00000505237.1:n.*1376+31G=
ENST00000680702.1:n.461+31G=
ENST00000680704.1:c.1187+31G= ENSP00000506453.1:n.1187+31G=
ENST00000680872.1:c.*682+31G= ENSP00000506605.1:n.*682+31G=
ENST00000680944.1:n.951+31G=
ENST00000680958.1:n.1463+31G=
ENST00000681096.1:c.1097+31G= ENSP00000506052.1:n.1097+31G=
ENST00000681154.1:c.1469+31G= ENSP00000505866.1:n.1469+31G=
ENST00000681160.1:c.1187+31G= ENSP00000504905.1:n.1187+31G=
ENST00000681317.1:c.1556+31G= ENSP00000505190.1:n.1556+31G=
ENST00000681478.1:c.*1376+31G= ENSP00000505041.1:n.*1376+31G=
ENST00000681510.1:c.1406+31G= ENSP00000505594.1:n.1406+31G=
ENST00000681600.1:n.651+31G=
ENST00000681661.1:c.*537+31G= ENSP00000506596.1:n.*537+31G=
ENST00000681830.1:c.1105+31G= ENSP00000505322.1:n.1105+31G=
ENST00000681897.1:n.808+31G=
ENST00000681902.1:c.1556+31G= ENSP00000505328.1:n.1556+31G=
ENST00000681917.1:c.1025+31G= ENSP00000505944.1:n.1025+31G=
ENST00000681943.1:c.1422+31G= ENSP00000504889.1:n.1422+31G=
ENST00000681946.1:c.*537+31G= ENSP00000505563.1:n.*537+31G=
ENST00000291074.9:c.1469+31G= ENSP00000291074.5:n.1469+31G=
ENST00000389040.9:c.1412+31G= ENSP00000373692.5:n.1412+31G=
ENST00000401468.7:c.725+31G= ENSP00000384294.3:n.725+31G=
ENST00000437048.6:c.1556+31G= ENSP00000401435.2:n.1556+31G=
ENST00000571805.5:c.1556+31G= ENSP00000459312.1:n.1556+31G=
ENST00000572607.1:n.184+31G=
ENST00000573028.5:c.*1003+31G= ENSP00000458311.1:n.*1003+31G=
ENST00000574029.5:c.207-44833G= ENSP00000459159.1:n.207-44833G=
ENST00000576149.5:n.1326+31G=
NM_001128159.2:c.1556+31G= NP_001121631.1:n.1556+31G=
NM_018289.3:c.1469+31G= NP_060759.2:n.1469+31G=
XM_011523953.1:c.962+31G= XP_011522255.1:n.962+31G=
XR_934061.1:n.1853+31G=
XR_934062.1:n.1608+31G=
NM_001366253.1:c.1556+31G= NP_001353182.1:n.1556+31G=
NM_001366254.1:c.962+31G= NP_001353183.1:n.962+31G=
XM_017024817.2:c.1406+31G= XP_016880306.1:n.1406+31G=
XM_017024818.1:c.1187+31G= XP_016880307.1:n.1187+31G=
XR_001752553.2:n.1693+31G=
XR_934061.3:n.1843+31G=
XR_934062.2:n.1598+31G=
NM_001128159.3:c.1556+31G= MANE Select NP_001121631.1:n.1556+31G=
NM_001366253.2:c.1556+31G= NP_001353182.1:n.1556+31G=
NM_001366254.2:c.962+31G= NP_001353183.1:n.962+31G=
NM_018289.4:c.1469+31G= NP_060759.2:n.1469+31G=