Canonical Allele Identifier: CA354577015
Gene: UBA5 HGNC NCBI
NPHP3-ACAD11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.132675907A>C , CM000665.2:g.132675907A>C GRCh38
NC_000003.11:g.132394751A>C , CM000665.1:g.132394751A>C GRCh37
NC_000003.10:g.133877441A>C NCBI36
NG_052968.1:g.26462A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000683741.1:c.1286A>C (UBA5) ENSP00000507396.1:p.Tyr429Ser
ENST00000356232.10:c.1115A>C (UBA5) MANE Select ENSP00000348565.4:p.Tyr372Ser
ENST00000264991.8:c.947A>C (UBA5) ENSP00000264991.4:p.Tyr316Ser
ENST00000356232.8:c.1115A>C (UBA5) ENSP00000348565.4:p.Tyr372Ser
ENST00000468227.5:n.2546A>C (UBA5)
ENST00000471702.2:c.*1980+6007T>G (NPHP3-ACAD11) ENSP00000419763.1:n.*1980+6007T>G
ENST00000473651.5:c.1024+227A>C (UBA5) ENSP00000424984.1:n.1024+227A>C
ENST00000493720.6:c.1115A>C (UBA5) ENSP00000417879.2:p.Tyr372Ser
ENST00000494112.1:n.390A>C (UBA5)
ENST00000494238.6:c.947A>C (UBA5) ENSP00000418807.2:p.Tyr316Ser
ENST00000632629.1:c.636+6007T>G (NPHP3-ACAD11)
NM_024818.3:c.1115A>C (UBA5) NP_079094.1:p.Tyr372Ser
NM_198329.2:c.947A>C (UBA5) NP_938143.1:p.Tyr316Ser
NR_037804.1:n.3995+6007T>G (NPHP3-ACAD11)
XM_006713752.2:c.779A>C (UBA5) XP_006713815.1:p.Tyr260Ser
XM_011513183.1:c.974A>C (UBA5) XP_011511485.1:p.Tyr325Ser
XM_011513184.1:c.947A>C (UBA5) XP_011511486.1:p.Tyr316Ser
XM_011513185.1:c.845A>C (UBA5) XP_011511487.1:p.Tyr282Ser
NM_001320210.1:c.947A>C (UBA5) NP_001307139.1:p.Tyr316Ser
NM_001321238.1:c.845A>C (UBA5) NP_001308167.1:p.Tyr282Ser
NM_001321239.1:c.779A>C (UBA5) NP_001308168.1:p.Tyr260Ser
NM_024818.4:c.1115A>C (UBA5) NP_079094.1:p.Tyr372Ser
NM_198329.3:c.947A>C (UBA5) NP_938143.1:p.Tyr316Ser
XR_001740272.1:n.1581A>C (UBA5)
NM_024818.5:c.1115A>C (UBA5) NP_079094.1:p.Tyr372Ser
NM_001320210.2:c.947A>C (UBA5) NP_001307139.1:p.Tyr316Ser
NM_001321238.2:c.845A>C (UBA5) NP_001308167.1:p.Tyr282Ser
NM_024818.6:c.1115A>C (UBA5) MANE Select NP_079094.1:p.Tyr372Ser
NM_198329.4:c.947A>C (UBA5) NP_938143.1:p.Tyr316Ser