Canonical Allele Identifier: CA2242366349
Gene: VPS53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.532911G= , CM000679.2:g.532911G= GRCh38
NC_000017.10:g.436151G= , CM000679.1:g.436151G= GRCh37
NC_000017.9:g.382901G= NCBI36
NG_034190.1:g.186946C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291074.10:c.1929C= ENSP00000291074.5:p.Asn643=
ENST00000437048.7:c.2016C= MANE Select ENSP00000401435.2:p.Asn672=
ENST00000571805.6:c.2016C= ENSP00000459312.1:p.Asn672=
ENST00000572334.7:c.1647C= ENSP00000506188.1:p.Asn549=
ENST00000679817.1:c.246C= ENSP00000505032.1:p.Asn82=
ENST00000680128.1:c.1812C= ENSP00000506159.1:p.Asn604=
ENST00000680465.1:c.2016C= ENSP00000505997.1:p.Asn672=
ENST00000680641.1:c.*3265C= ENSP00000505237.1:n.*3265C=
ENST00000680704.1:c.1647C= ENSP00000506453.1:p.Asn549=
ENST00000680872.1:c.*1142C= ENSP00000506605.1:n.*1142C=
ENST00000681050.1:c.229C=
ENST00000681096.1:c.1557C= ENSP00000506052.1:p.Asn519=
ENST00000681103.1:c.246C= ENSP00000505892.1:p.Asn82=
ENST00000681160.1:c.1647C= ENSP00000504905.1:p.Asn549=
ENST00000681317.1:c.2015+4117C= ENSP00000505190.1:n.2015+4117C=
ENST00000681478.1:c.*1836C= ENSP00000505041.1:n.*1836C=
ENST00000681510.1:c.1866C= ENSP00000505594.1:p.Asn622=
ENST00000681600.1:n.1111C=
ENST00000681661.1:c.*997C= ENSP00000506596.1:n.*997C=
ENST00000681858.1:c.246C= ENSP00000505044.1:p.Asn82=
ENST00000681917.1:c.1485C= ENSP00000505944.1:p.Asn495=
ENST00000681943.1:c.1734C= ENSP00000504889.1:n.1734C=
ENST00000681946.1:c.*997C= ENSP00000505563.1:n.*997C=
ENST00000291074.9:c.1929C= ENSP00000291074.5:p.Asn643=
ENST00000389040.9:c.1819C= ENSP00000373692.5:n.1819C=
ENST00000401468.7:c.1185C= ENSP00000384294.3:p.Asn395=
ENST00000437048.6:c.2016C= ENSP00000401435.2:p.Asn672=
ENST00000570771.1:n.83C=
ENST00000571805.5:c.2016C= ENSP00000459312.1:p.Asn672=
ENST00000573028.5:c.*1463C= ENSP00000458311.1:n.*1463C=
ENST00000574029.5:c.207-15272C= ENSP00000459159.1:n.207-15272C=
ENST00000576149.5:n.1786C=
NM_001128159.2:c.2016C= NP_001121631.1:p.Asn672=
NM_018289.3:c.1929C= NP_060759.2:p.Asn643=
XM_011523953.1:c.1422C= XP_011522255.1:p.Asn474=
XR_934061.1:n.2313C=
XR_934133.1:n.291-7478G=
NM_001366253.1:c.2016C= NP_001353182.1:p.Asn672=
NM_001366254.1:c.1422C= NP_001353183.1:p.Asn474=
XM_017024817.2:c.1866C= XP_016880306.1:p.Asn622=
XM_017024818.1:c.1647C= XP_016880307.1:p.Asn549=
XR_001752553.2:n.2153C=
XR_934061.3:n.2303C=
NM_001128159.3:c.2016C= MANE Select NP_001121631.1:p.Asn672=
NM_001366253.2:c.2016C= NP_001353182.1:p.Asn672=
NM_001366254.2:c.1422C= NP_001353183.1:p.Asn474=
NM_018289.4:c.1929C= NP_060759.2:p.Asn643=