Canonical Allele Identifier: CA2551795714
Gene: UBA5 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132675450_132675451insCTTC , CM000665.2:g.132675450_132675451insCTTC GRCh38
NC_000003.11:g.132394294_132394295insCTTC , CM000665.1:g.132394294_132394295insCTTC GRCh37
NC_000003.10:g.133876984_133876985insCTTC NCBI36
NG_052968.1:g.26005_26006insCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000683741.1:c.1119+67_1119+68insCTTC (UBA5) ENSP00000507396.1:n.1119+67_1119+68insCTTC
ENST00000356232.10:c.948+67_948+68insCTTC (UBA5) MANE Select ENSP00000348565.4:n.948+67_948+68insCTTC
ENST00000264991.8:c.780+67_780+68insCTTC (UBA5) ENSP00000264991.4:n.780+67_780+68insCTTC
ENST00000356232.8:c.948+67_948+68insCTTC (UBA5) ENSP00000348565.4:n.948+67_948+68insCTTC
ENST00000468227.5:n.2379+67_2379+68insCTTC (UBA5)
ENST00000471702.2:c.*1980+6463_*1980+6464insGAAG (NPHP3-ACAD11) ENSP00000419763.1:n.*1980+6463_*1980+6464insGAAG
ENST00000473651.5:c.948+67_948+68insCTTC (UBA5) ENSP00000424984.1:n.948+67_948+68insCTTC
ENST00000493720.6:c.948+67_948+68insCTTC (UBA5) ENSP00000417879.2:n.948+67_948+68insCTTC
ENST00000494112.1:n.69_70insCTTC (UBA5)
ENST00000494238.6:c.780+67_780+68insCTTC (UBA5) ENSP00000418807.2:n.780+67_780+68insCTTC
ENST00000632629.1:c.636+6463_636+6464insGAAG (NPHP3-ACAD11)
NM_024818.3:c.948+67_948+68insCTTC (UBA5) NP_079094.1:n.948+67_948+68insCTTC
NM_198329.2:c.780+67_780+68insCTTC (UBA5) NP_938143.1:n.780+67_780+68insCTTC
NR_037804.1:n.3995+6463_3995+6464insGAAG (NPHP3-ACAD11)
XM_006713752.2:c.612+67_612+68insCTTC (UBA5) XP_006713815.1:n.612+67_612+68insCTTC
XM_011513183.1:c.807+67_807+68insCTTC (UBA5) XP_011511485.1:n.807+67_807+68insCTTC
XM_011513184.1:c.780+67_780+68insCTTC (UBA5) XP_011511486.1:n.780+67_780+68insCTTC
XM_011513185.1:c.678+67_678+68insCTTC (UBA5) XP_011511487.1:n.678+67_678+68insCTTC
NM_001320210.1:c.780+67_780+68insCTTC (UBA5) NP_001307139.1:n.780+67_780+68insCTTC
NM_001321238.1:c.678+67_678+68insCTTC (UBA5) NP_001308167.1:n.678+67_678+68insCTTC
NM_001321239.1:c.612+67_612+68insCTTC (UBA5) NP_001308168.1:n.612+67_612+68insCTTC
NM_024818.4:c.948+67_948+68insCTTC (UBA5) NP_079094.1:n.948+67_948+68insCTTC
NM_198329.3:c.780+67_780+68insCTTC (UBA5) NP_938143.1:n.780+67_780+68insCTTC
XR_001740272.1:n.1415-155_1415-154insCTTC (UBA5)
NM_024818.5:c.948+67_948+68insCTTC (UBA5) NP_079094.1:n.948+67_948+68insCTTC
NM_001320210.2:c.780+67_780+68insCTTC (UBA5) NP_001307139.1:n.780+67_780+68insCTTC
NM_001321238.2:c.678+67_678+68insCTTC (UBA5) NP_001308167.1:n.678+67_678+68insCTTC
NM_024818.6:c.948+67_948+68insCTTC (UBA5) MANE Select NP_079094.1:n.948+67_948+68insCTTC
NM_198329.4:c.780+67_780+68insCTTC (UBA5) NP_938143.1:n.780+67_780+68insCTTC