Canonical Allele Identifier: CA354575961
Gene: UBA5 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132675258A>T , CM000665.2:g.132675258A>T GRCh38
NC_000003.11:g.132394102A>T , CM000665.1:g.132394102A>T GRCh37
NC_000003.10:g.133876792A>T NCBI36
NG_052968.1:g.25813A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683741.1:c.994A>T (UBA5) ENSP00000507396.1:p.Asn332Tyr
ENST00000356232.10:c.823A>T (UBA5) MANE Select ENSP00000348565.4:p.Asn275Tyr
ENST00000264991.8:c.655A>T (UBA5) ENSP00000264991.4:p.Asn219Tyr
ENST00000356232.8:c.823A>T (UBA5) ENSP00000348565.4:p.Asn275Tyr
ENST00000468227.5:n.2254A>T (UBA5)
ENST00000471702.2:c.*1980+6656T>A (NPHP3-ACAD11) ENSP00000419763.1:n.*1980+6656T>A
ENST00000473651.5:c.823A>T (UBA5) ENSP00000424984.1:p.Asn275Tyr
ENST00000493720.6:c.823A>T (UBA5) ENSP00000417879.2:p.Asn275Tyr
ENST00000494238.6:c.655A>T (UBA5) ENSP00000418807.2:p.Asn219Tyr
ENST00000632629.1:c.636+6656T>A (NPHP3-ACAD11)
NM_024818.3:c.823A>T (UBA5) NP_079094.1:p.Asn275Tyr
NM_198329.2:c.655A>T (UBA5) NP_938143.1:p.Asn219Tyr
NR_037804.1:n.3995+6656T>A (NPHP3-ACAD11)
XM_006713752.2:c.487A>T (UBA5) XP_006713815.1:p.Asn163Tyr
XM_011513183.1:c.682A>T (UBA5) XP_011511485.1:p.Asn228Tyr
XM_011513184.1:c.655A>T (UBA5) XP_011511486.1:p.Asn219Tyr
XM_011513185.1:c.553A>T (UBA5) XP_011511487.1:p.Asn185Tyr
NM_001320210.1:c.655A>T (UBA5) NP_001307139.1:p.Asn219Tyr
NM_001321238.1:c.553A>T (UBA5) NP_001308167.1:p.Asn185Tyr
NM_001321239.1:c.487A>T (UBA5) NP_001308168.1:p.Asn163Tyr
NM_024818.4:c.823A>T (UBA5) NP_079094.1:p.Asn275Tyr
NM_198329.3:c.655A>T (UBA5) NP_938143.1:p.Asn219Tyr
XR_001740272.1:n.1415-347A>T (UBA5)
NM_024818.5:c.823A>T (UBA5) NP_079094.1:p.Asn275Tyr
NM_001320210.2:c.655A>T (UBA5) NP_001307139.1:p.Asn219Tyr
NM_001321238.2:c.553A>T (UBA5) NP_001308167.1:p.Asn185Tyr
NM_024818.6:c.823A>T (UBA5) MANE Select NP_079094.1:p.Asn275Tyr
NM_198329.4:c.655A>T (UBA5) NP_938143.1:p.Asn219Tyr