Canonical Allele Identifier: CA354577164
Gene: UBA5 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132676483G>C , CM000665.2:g.132676483G>C GRCh38
NC_000003.11:g.132395327G>C , CM000665.1:g.132395327G>C GRCh37
NC_000003.10:g.133878017G>C NCBI36
NG_052968.1:g.27038G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000683741.1:c.1343G>C (UBA5) ENSP00000507396.1:p.Gly448Ala
ENST00000356232.10:c.1172G>C (UBA5) MANE Select ENSP00000348565.4:p.Gly391Ala
ENST00000264991.8:c.1004G>C (UBA5) ENSP00000264991.4:p.Gly335Ala
ENST00000356232.8:c.1172G>C (UBA5) ENSP00000348565.4:p.Gly391Ala
ENST00000468227.5:n.2603G>C (UBA5)
ENST00000471702.2:c.*1980+5431C>G (NPHP3-ACAD11) ENSP00000419763.1:n.*1980+5431C>G
ENST00000473651.5:c.*21G>C (UBA5) ENSP00000424984.1:n.*21G>C
ENST00000493720.6:c.1132-372G>C (UBA5) ENSP00000417879.2:n.1132-372G>C
ENST00000494112.1:n.447G>C (UBA5)
ENST00000494238.6:c.1004G>C (UBA5) ENSP00000418807.2:p.Gly335Ala
ENST00000632629.1:c.636+5431C>G (NPHP3-ACAD11)
NM_024818.3:c.1172G>C (UBA5) NP_079094.1:p.Gly391Ala
NM_198329.2:c.1004G>C (UBA5) NP_938143.1:p.Gly335Ala
NR_037804.1:n.3995+5431C>G (NPHP3-ACAD11)
XM_006713752.2:c.836G>C (UBA5) XP_006713815.1:p.Gly279Ala
XM_011513183.1:c.1031G>C (UBA5) XP_011511485.1:p.Gly344Ala
XM_011513184.1:c.1004G>C (UBA5) XP_011511486.1:p.Gly335Ala
XM_011513185.1:c.902G>C (UBA5) XP_011511487.1:p.Gly301Ala
NM_001320210.1:c.1004G>C (UBA5) NP_001307139.1:p.Gly335Ala
NM_001321238.1:c.902G>C (UBA5) NP_001308167.1:p.Gly301Ala
NM_001321239.1:c.836G>C (UBA5) NP_001308168.1:p.Gly279Ala
NM_024818.4:c.1172G>C (UBA5) NP_079094.1:p.Gly391Ala
NM_198329.3:c.1004G>C (UBA5) NP_938143.1:p.Gly335Ala
XR_001740272.1:n.1638G>C (UBA5)
NM_024818.5:c.1172G>C (UBA5) NP_079094.1:p.Gly391Ala
NM_001320210.2:c.1004G>C (UBA5) NP_001307139.1:p.Gly335Ala
NM_001321238.2:c.902G>C (UBA5) NP_001308167.1:p.Gly301Ala
NM_024818.6:c.1172G>C (UBA5) MANE Select NP_079094.1:p.Gly391Ala
NM_198329.4:c.1004G>C (UBA5) NP_938143.1:p.Gly335Ala