Canonical Allele Identifier: CA2242366333
Gene: VPS53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.532874A= , CM000679.2:g.532874A= GRCh38
NC_000017.10:g.436114A= , CM000679.1:g.436114A= GRCh37
NC_000017.9:g.382864A= NCBI36
NG_034190.1:g.186983T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291074.10:c.1966T= ENSP00000291074.5:p.Cys656=
ENST00000437048.7:c.2053T= MANE Select ENSP00000401435.2:p.Cys685=
ENST00000571805.6:c.2053T= ENSP00000459312.1:p.Cys685=
ENST00000572334.7:c.1684T= ENSP00000506188.1:p.Cys562=
ENST00000679817.1:c.283T= ENSP00000505032.1:p.Cys95=
ENST00000680128.1:c.1849T= ENSP00000506159.1:p.Cys617=
ENST00000680465.1:c.2053T= ENSP00000505997.1:p.Cys685=
ENST00000680641.1:c.*3302T= ENSP00000505237.1:n.*3302T=
ENST00000680704.1:c.1684T= ENSP00000506453.1:p.Cys562=
ENST00000680872.1:c.*1179T= ENSP00000506605.1:n.*1179T=
ENST00000681050.1:c.266T=
ENST00000681096.1:c.1594T= ENSP00000506052.1:p.Cys532=
ENST00000681103.1:c.283T= ENSP00000505892.1:p.Cys95=
ENST00000681160.1:c.1684T= ENSP00000504905.1:p.Cys562=
ENST00000681317.1:c.2015+4154T= ENSP00000505190.1:n.2015+4154T=
ENST00000681478.1:c.*1873T= ENSP00000505041.1:n.*1873T=
ENST00000681510.1:c.1903T= ENSP00000505594.1:p.Cys635=
ENST00000681600.1:n.1148T=
ENST00000681661.1:c.*1034T= ENSP00000506596.1:n.*1034T=
ENST00000681858.1:c.283T= ENSP00000505044.1:p.Cys95=
ENST00000681917.1:c.1522T= ENSP00000505944.1:p.Cys508=
ENST00000681943.1:c.1771T= ENSP00000504889.1:n.1771T=
ENST00000681946.1:c.*1034T= ENSP00000505563.1:n.*1034T=
ENST00000291074.9:c.1966T= ENSP00000291074.5:p.Cys656=
ENST00000389040.9:c.1856T= ENSP00000373692.5:n.1856T=
ENST00000401468.7:c.1222T= ENSP00000384294.3:p.Cys408=
ENST00000437048.6:c.2053T= ENSP00000401435.2:p.Cys685=
ENST00000570771.1:n.120T=
ENST00000571805.5:c.2053T= ENSP00000459312.1:p.Cys685=
ENST00000573028.5:c.*1500T= ENSP00000458311.1:n.*1500T=
ENST00000574029.5:c.207-15235T= ENSP00000459159.1:n.207-15235T=
ENST00000576149.5:n.1823T=
NM_001128159.2:c.2053T= NP_001121631.1:p.Cys685=
NM_018289.3:c.1966T= NP_060759.2:p.Cys656=
XM_011523953.1:c.1459T= XP_011522255.1:p.Cys487=
XR_934061.1:n.2350T=
XR_934133.1:n.291-7515A=
NM_001366253.1:c.2053T= NP_001353182.1:p.Cys685=
NM_001366254.1:c.1459T= NP_001353183.1:p.Cys487=
XM_017024817.2:c.1903T= XP_016880306.1:p.Cys635=
XM_017024818.1:c.1684T= XP_016880307.1:p.Cys562=
XR_001752553.2:n.2190T=
XR_934061.3:n.2340T=
NM_001128159.3:c.2053T= MANE Select NP_001121631.1:p.Cys685=
NM_001366253.2:c.2053T= NP_001353182.1:p.Cys685=
NM_001366254.2:c.1459T= NP_001353183.1:p.Cys487=
NM_018289.4:c.1966T= NP_060759.2:p.Cys656=