Linked Data
ClinVar Variation Id:
265751
ClinVar RCV Id:
RCV000256096
dbSNP Id:
rs886039758
PubMed:
PMID:27545681
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.132675627_132675628insC , CM000665.2:g.132675627_132675628insC | GRCh38 |
| NC_000003.11:g.132394471_132394472insC , CM000665.1:g.132394471_132394472insC | GRCh37 |
| NC_000003.10:g.133877161_133877162insC | NCBI36 |
| NG_052968.1:g.26182_26183insC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000683741.1:c.1142_1143insC (UBA5) | ENSP00000507396.1:p.Lys381AsnfsTer14 | |
| ENST00000356232.10:c.971_972insC (UBA5) MANE Select | ENSP00000348565.4:p.Lys324AsnfsTer14 | |
| ENST00000264991.8:c.803_804insC (UBA5) | ENSP00000264991.4:p.Lys268AsnfsTer14 | |
| ENST00000356232.8:c.971_972insC (UBA5) | ENSP00000348565.4:p.Lys324AsnfsTer14 | |
| ENST00000468227.5:n.2402_2403insC (UBA5) | ||
| ENST00000471702.2:c.*1980+6286_*1980+6287insG (NPHP3-ACAD11) | ENSP00000419763.1:n.*1980+6286_*1980+6287... | |
| ENST00000473651.5:c.971_972insC (UBA5) | ENSP00000424984.1:p.Lys324AsnfsTer14 | |
| ENST00000493720.6:c.971_972insC (UBA5) | ENSP00000417879.2:p.Lys324AsnfsTer14 | |
| ENST00000494112.1:n.246_247insC (UBA5) | ||
| ENST00000494238.6:c.803_804insC (UBA5) | ENSP00000418807.2:p.Lys268AsnfsTer14 | |
| ENST00000632629.1:c.636+6286_636+6287insG (NPHP3-ACAD11) | ||
| NM_024818.3:c.971_972insC (UBA5) | NP_079094.1:p.Lys324AsnfsTer14 | |
| NM_198329.2:c.803_804insC (UBA5) | NP_938143.1:p.Lys268AsnfsTer14 | |
| NR_037804.1:n.3995+6286_3995+6287insG (NPHP3-ACAD11) | ||
| XM_006713752.2:c.635_636insC (UBA5) | XP_006713815.1:p.Lys212AsnfsTer14 | |
| XM_011513183.1:c.830_831insC (UBA5) | XP_011511485.1:p.Lys277AsnfsTer14 | |
| XM_011513184.1:c.803_804insC (UBA5) | XP_011511486.1:p.Lys268AsnfsTer14 | |
| XM_011513185.1:c.701_702insC (UBA5) | XP_011511487.1:p.Lys234AsnfsTer14 | |
| NM_001320210.1:c.803_804insC (UBA5) | NP_001307139.1:p.Lys268AsnfsTer14 | |
| NM_001321238.1:c.701_702insC (UBA5) | NP_001308167.1:p.Lys234AsnfsTer14 | |
| NM_001321239.1:c.635_636insC (UBA5) | NP_001308168.1:p.Lys212AsnfsTer14 | |
| NM_024818.4:c.971_972insC (UBA5) | NP_079094.1:p.Lys324AsnfsTer14 | |
| NM_198329.3:c.803_804insC (UBA5) | NP_938143.1:p.Lys268AsnfsTer14 | |
| XR_001740272.1:n.1437_1438insC (UBA5) | ||
| NM_024818.5:c.971_972insC (UBA5) | NP_079094.1:p.Lys324AsnfsTer14 | |
| NM_001320210.2:c.803_804insC (UBA5) | NP_001307139.1:p.Lys268AsnfsTer14 | |
| NM_001321238.2:c.701_702insC (UBA5) | NP_001308167.1:p.Lys234AsnfsTer14 | |
| NM_024818.6:c.971_972insC (UBA5) MANE Select | NP_079094.1:p.Lys324AsnfsTer14 | |
| NM_198329.4:c.803_804insC (UBA5) | NP_938143.1:p.Lys268AsnfsTer14 |