Canonical Allele Identifier: CA2242382294
Gene: VPS53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.562522G= , CM000679.2:g.562522G= GRCh38
NC_000017.10:g.465762G= , CM000679.1:g.465762G= GRCh37
NC_000017.9:g.412512G= NCBI36
NG_034190.1:g.157335C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291074.10:c.1450C= ENSP00000291074.5:p.Leu484=
ENST00000437048.7:c.1537C= MANE Select ENSP00000401435.2:p.Leu513=
ENST00000571805.6:c.1537C= ENSP00000459312.1:p.Leu513=
ENST00000572334.7:c.1168C= ENSP00000506188.1:p.Leu390=
ENST00000572607.2:n.367C=
ENST00000679361.1:c.1537C= ENSP00000504978.1:p.Leu513=
ENST00000679959.1:c.1070C= ENSP00000506180.1:n.1070C=
ENST00000680069.1:c.1537C= ENSP00000505145.1:p.Leu513=
ENST00000680114.1:c.1063C= ENSP00000505327.1:p.Leu355=
ENST00000680128.1:c.1333C= ENSP00000506159.1:p.Leu445=
ENST00000680274.1:n.1099C=
ENST00000680465.1:c.1537C= ENSP00000505997.1:p.Leu513=
ENST00000680641.1:c.*1357C= ENSP00000505237.1:n.*1357C=
ENST00000680702.1:n.442C=
ENST00000680704.1:c.1168C= ENSP00000506453.1:p.Leu390=
ENST00000680872.1:c.*663C= ENSP00000506605.1:n.*663C=
ENST00000680944.1:n.932C=
ENST00000680958.1:n.1444C=
ENST00000681096.1:c.1078C= ENSP00000506052.1:p.Leu360=
ENST00000681154.1:c.1450C= ENSP00000505866.1:p.Leu484=
ENST00000681160.1:c.1168C= ENSP00000504905.1:p.Leu390=
ENST00000681317.1:c.1537C= ENSP00000505190.1:p.Leu513=
ENST00000681478.1:c.*1357C= ENSP00000505041.1:n.*1357C=
ENST00000681510.1:c.1387C= ENSP00000505594.1:p.Leu463=
ENST00000681600.1:n.632C=
ENST00000681661.1:c.*518C= ENSP00000506596.1:n.*518C=
ENST00000681830.1:c.1086C= ENSP00000505322.1:n.1086C=
ENST00000681897.1:n.789C=
ENST00000681902.1:c.1537C= ENSP00000505328.1:p.Leu513=
ENST00000681917.1:c.1006C= ENSP00000505944.1:p.Leu336=
ENST00000681943.1:c.1403C= ENSP00000504889.1:n.1403C=
ENST00000681946.1:c.*518C= ENSP00000505563.1:n.*518C=
ENST00000291074.9:c.1450C= ENSP00000291074.5:p.Leu484=
ENST00000389040.9:c.1393C= ENSP00000373692.5:p.Leu465=
ENST00000401468.7:c.706C= ENSP00000384294.3:p.Leu236=
ENST00000437048.6:c.1537C= ENSP00000401435.2:p.Leu513=
ENST00000571805.5:c.1537C= ENSP00000459312.1:p.Leu513=
ENST00000572607.1:n.165C=
ENST00000573028.5:c.*984C= ENSP00000458311.1:n.*984C=
ENST00000574029.5:c.207-44883C= ENSP00000459159.1:n.207-44883C=
ENST00000576149.5:n.1307C=
NM_001128159.2:c.1537C= NP_001121631.1:p.Leu513=
NM_018289.3:c.1450C= NP_060759.2:p.Leu484=
XM_011523953.1:c.943C= XP_011522255.1:p.Leu315=
XR_934061.1:n.1834C=
XR_934062.1:n.1589C=
NM_001366253.1:c.1537C= NP_001353182.1:p.Leu513=
NM_001366254.1:c.943C= NP_001353183.1:p.Leu315=
XM_017024817.2:c.1387C= XP_016880306.1:p.Leu463=
XM_017024818.1:c.1168C= XP_016880307.1:p.Leu390=
XR_001752553.2:n.1674C=
XR_934061.3:n.1824C=
XR_934062.2:n.1579C=
NM_001128159.3:c.1537C= MANE Select NP_001121631.1:p.Leu513=
NM_001366253.2:c.1537C= NP_001353182.1:p.Leu513=
NM_001366254.2:c.943C= NP_001353183.1:p.Leu315=
NM_018289.4:c.1450C= NP_060759.2:p.Leu484=