Canonical Allele Identifier: CA2242366371
Gene: VPS53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.532970A= , CM000679.2:g.532970A= GRCh38
NC_000017.10:g.436210A= , CM000679.1:g.436210A= GRCh37
NC_000017.9:g.382960A= NCBI36
NG_034190.1:g.186887T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291074.10:c.1929-59T= ENSP00000291074.5:n.1929-59T=
ENST00000437048.7:c.2016-59T= MANE Select ENSP00000401435.2:n.2016-59T=
ENST00000571805.6:c.2016-59T= ENSP00000459312.1:n.2016-59T=
ENST00000572334.7:c.1647-59T= ENSP00000506188.1:n.1647-59T=
ENST00000679817.1:c.246-59T= ENSP00000505032.1:n.246-59T=
ENST00000680128.1:c.1812-59T= ENSP00000506159.1:n.1812-59T=
ENST00000680465.1:c.2016-59T= ENSP00000505997.1:n.2016-59T=
ENST00000680641.1:c.*3265-59T= ENSP00000505237.1:n.*3265-59T=
ENST00000680704.1:c.1647-59T= ENSP00000506453.1:n.1647-59T=
ENST00000680872.1:c.*1142-59T= ENSP00000506605.1:n.*1142-59T=
ENST00000681050.1:c.229-59T=
ENST00000681096.1:c.1557-59T= ENSP00000506052.1:n.1557-59T=
ENST00000681103.1:c.246-59T= ENSP00000505892.1:n.246-59T=
ENST00000681160.1:c.1647-59T= ENSP00000504905.1:n.1647-59T=
ENST00000681317.1:c.2015+4058T= ENSP00000505190.1:n.2015+4058T=
ENST00000681478.1:c.*1836-59T= ENSP00000505041.1:n.*1836-59T=
ENST00000681510.1:c.1866-59T= ENSP00000505594.1:n.1866-59T=
ENST00000681600.1:n.1111-59T=
ENST00000681661.1:c.*997-59T= ENSP00000506596.1:n.*997-59T=
ENST00000681858.1:c.246-59T= ENSP00000505044.1:n.246-59T=
ENST00000681917.1:c.1485-59T= ENSP00000505944.1:n.1485-59T=
ENST00000681943.1:c.1734-59T= ENSP00000504889.1:n.1734-59T=
ENST00000681946.1:c.*997-59T= ENSP00000505563.1:n.*997-59T=
ENST00000291074.9:c.1929-59T= ENSP00000291074.5:n.1929-59T=
ENST00000389040.9:c.1819-59T= ENSP00000373692.5:n.1819-59T=
ENST00000401468.7:c.1185-59T= ENSP00000384294.3:n.1185-59T=
ENST00000437048.6:c.2016-59T= ENSP00000401435.2:n.2016-59T=
ENST00000570771.1:n.24T=
ENST00000571805.5:c.2016-59T= ENSP00000459312.1:n.2016-59T=
ENST00000573028.5:c.*1463-59T= ENSP00000458311.1:n.*1463-59T=
ENST00000574029.5:c.207-15331T= ENSP00000459159.1:n.207-15331T=
ENST00000576149.5:n.1786-59T=
NM_001128159.2:c.2016-59T= NP_001121631.1:n.2016-59T=
NM_018289.3:c.1929-59T= NP_060759.2:n.1929-59T=
XM_011523953.1:c.1422-59T= XP_011522255.1:n.1422-59T=
XR_934061.1:n.2313-59T=
XR_934133.1:n.291-7419A=
NM_001366253.1:c.2016-59T= NP_001353182.1:n.2016-59T=
NM_001366254.1:c.1422-59T= NP_001353183.1:n.1422-59T=
XM_017024817.2:c.1866-59T= XP_016880306.1:n.1866-59T=
XM_017024818.1:c.1647-59T= XP_016880307.1:n.1647-59T=
XR_001752553.2:n.2153-59T=
XR_934061.3:n.2303-59T=
NM_001128159.3:c.2016-59T= MANE Select NP_001121631.1:n.2016-59T=
NM_001366253.2:c.2016-59T= NP_001353182.1:n.2016-59T=
NM_001366254.2:c.1422-59T= NP_001353183.1:n.1422-59T=
NM_018289.4:c.1929-59T= NP_060759.2:n.1929-59T=