Linked Data
ClinVar Variation Id:
597013
dbSNP Id:
rs755581358
ExAC:
15:25584280 T / C
gnomAD v2:
15-25584280-T-C
gnomAD v3:
15-25339133-T-C
gnomAD v4:
15-25339133-T-C
ERepo:
CA7435334/MONDO:0007113/032
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.25339133T>C , CM000677.2:g.25339133T>C | GRCh38 |
| NC_000015.9:g.25584280T>C , CM000677.1:g.25584280T>C | GRCh37 |
| NC_000015.8:g.23135373T>C | NCBI36 |
| NG_009268.1:g.104849A>G , LRG_15:g.104849A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000438097.6:c.*4A>G (UBE3A) | ENSP00000411258.1:n.*4A>G | |
| ENST00000635914.1:c.*948A>G (UBE3A) | ENSP00000490563.1:n.*948A>G | |
| ENST00000636667.1:c.*4A>G (UBE3A) | ENSP00000489625.1:n.*4A>G | |
| ENST00000637886.1:c.*4A>G (UBE3A) | ENSP00000490258.1:n.*4A>G | |
| ENST00000638011.1:c.*4A>G (UBE3A) | ENSP00000490111.1:n.*4A>G | |
| ENST00000638155.1:c.*4A>G (UBE3A) | ENSP00000490557.1:n.*4A>G | |
| ENST00000648336.2:c.*4A>G (UBE3A) MANE Select | ENSP00000497572.2:n.*4A>G | |
| ENST00000649550.1:c.*4A>G (UBE3A) | ENSP00000497549.1:n.*4A>G | |
| ENST00000650110.1:c.*4A>G (UBE3A) | ENSP00000497594.1:n.*4A>G | |
| ENST00000232165.7:c.*4A>G (UBE3A) | ENSP00000232165.5:n.*4A>G | |
| ENST00000428984.6:c.*4A>G (UBE3A) | ENSP00000401265.2:n.*4A>G | |
| ENST00000566215.5:c.*4A>G (UBE3A) | ENSP00000457771.1:n.*4A>G | |
| ENST00000614096.4:c.*4A>G (UBE3A) | ENSP00000481796.1:n.*4A>G | |
| ENST00000626176.2:c.434A>G (UBE3A) | ||
| ENST00000630424.2:c.*4A>G (UBE3A) | ENSP00000486349.1:n.*4A>G | |
| NM_000462.3:c.*4A>G (UBE3A) | NP_000453.2:n.*4A>G | |
| NM_130838.1:c.*4A>G , LRG_15t1:c.*4A>G (UBE3A) | NP_570853.1:n.*4A>G | |
| NM_130839.2:c.*4A>G (UBE3A) | NP_570854.1:n.*4A>G | |
| XM_005268267.3:c.*4A>G (UBE3A) | XP_005268324.1:n.*4A>G | |
| XM_005268268.3:c.*4A>G (UBE3A) | XP_005268325.1:n.*4A>G | |
| XM_005268269.3:c.*4A>G (UBE3A) | XP_005268326.1:n.*4A>G | |
| XM_005268270.3:c.*4A>G (UBE3A) | XP_005268327.1:n.*4A>G | |
| XM_005268271.3:c.*4A>G (UBE3A) | XP_005268328.1:n.*4A>G | |
| XM_006720673.2:c.*4A>G (UBE3A) | XP_006720736.1:n.*4A>G | |
| XM_006720674.2:c.*4A>G (UBE3A) | XP_006720737.1:n.*4A>G | |
| XM_006720675.2:c.*4A>G (UBE3A) | XP_006720738.1:n.*4A>G | |
| XM_006720676.2:c.*4A>G (UBE3A) | XP_006720739.1:n.*4A>G | |
| XM_011521994.1:c.*4A>G (UBE3A) | XP_011520296.1:n.*4A>G | |
| XM_011521995.1:c.*4A>G (UBE3A) | XP_011520297.1:n.*4A>G | |
| XM_011521996.1:c.*4A>G (UBE3A) | XP_011520298.1:n.*4A>G | |
| NM_000462.5:c.*4A>G (UBE3A) | NP_000453.2:n.*4A>G | |
| NM_001354505.1:c.*4A>G (UBE3A) | NP_001341434.1:n.*4A>G | |
| NM_001354506.1:c.*4A>G (UBE3A) | NP_001341435.1:n.*4A>G | |
| NM_001354507.1:c.*4A>G (UBE3A) | NP_001341436.1:n.*4A>G | |
| NM_001354508.1:c.*4A>G (UBE3A) | NP_001341437.1:n.*4A>G | |
| NM_001354509.1:c.*4A>G (UBE3A) | NP_001341438.1:n.*4A>G | |
| NM_001354511.1:c.*4A>G (UBE3A) | NP_001341440.1:n.*4A>G | |
| NM_001354512.1:c.*4A>G (UBE3A) | NP_001341441.1:n.*4A>G | |
| NM_001354513.1:c.*4A>G (UBE3A) | NP_001341442.1:n.*4A>G | |
| NM_001354523.1:c.*4A>G (UBE3A) | NP_001341452.1:n.*4A>G | |
| NM_001354526.1:c.*4A>G (UBE3A) | NP_001341455.1:n.*4A>G | |
| NM_001354538.1:c.*4A>G (UBE3A) | NP_001341467.1:n.*4A>G | |
| NM_001354539.1:c.*4A>G (UBE3A) | NP_001341468.1:n.*4A>G | |
| NM_001354540.1:c.*4A>G (UBE3A) | NP_001341469.1:n.*4A>G | |
| NM_001354541.1:c.*4A>G (UBE3A) | NP_001341470.1:n.*4A>G | |
| NM_001354542.1:c.*4A>G (UBE3A) | NP_001341471.1:n.*4A>G | |
| NM_001354543.1:c.*4A>G (UBE3A) | NP_001341472.1:n.*4A>G | |
| NM_001354544.1:c.*4A>G (UBE3A) | NP_001341473.1:n.*4A>G | |
| NM_001354545.1:c.*4A>G (UBE3A) | NP_001341474.1:n.*4A>G | |
| NM_001354546.1:c.*4A>G (UBE3A) | NP_001341475.1:n.*4A>G | |
| NM_001354547.1:c.*4A>G (UBE3A) | NP_001341476.1:n.*4A>G | |
| NM_001354548.1:c.*4A>G (UBE3A) | NP_001341477.1:n.*4A>G | |
| NM_001354549.1:c.*4A>G (UBE3A) | NP_001341478.1:n.*4A>G | |
| NM_001354550.1:c.*4A>G (UBE3A) | NP_001341479.1:n.*4A>G | |
| NM_001354551.1:c.*4A>G (UBE3A) | NP_001341480.1:n.*4A>G | |
| NM_130838.3:c.*4A>G (UBE3A) | NP_570853.1:n.*4A>G | |
| NM_130839.4:c.*4A>G (UBE3A) | NP_570854.1:n.*4A>G | |
| NR_146177.1:n.18393-52463T>C (SNHG14) | ||
| NR_148916.1:n.3167A>G (UBE3A) | ||
| XM_011521995.3:c.*4A>G (UBE3A) | XP_011520297.1:n.*4A>G | |
| XM_017022547.2:c.*4A>G (UBE3A) | XP_016878036.1:n.*4A>G | |
| XM_017022548.2:c.*4A>G (UBE3A) | XP_016878037.1:n.*4A>G | |
| XM_017022550.2:c.*4A>G (UBE3A) | XP_016878039.1:n.*4A>G | |
| XM_017022556.2:c.*4A>G (UBE3A) | XP_016878045.1:n.*4A>G | |
| XM_024450043.1:c.*4A>G (UBE3A) | XP_024305811.1:n.*4A>G | |
| XM_024450044.1:c.*4A>G (UBE3A) | XP_024305812.1:n.*4A>G | |
| NM_001354506.2:c.*4A>G (UBE3A) | NP_001341435.1:n.*4A>G | |
| NM_001354507.2:c.*4A>G (UBE3A) | NP_001341436.1:n.*4A>G | |
| NM_001354508.2:c.*4A>G (UBE3A) | NP_001341437.1:n.*4A>G | |
| NM_001354509.2:c.*4A>G (UBE3A) | NP_001341438.1:n.*4A>G | |
| NM_001354511.2:c.*4A>G (UBE3A) | NP_001341440.1:n.*4A>G | |
| NM_001354512.2:c.*4A>G (UBE3A) | NP_001341441.1:n.*4A>G | |
| NM_001354513.2:c.*4A>G (UBE3A) | NP_001341442.1:n.*4A>G | |
| NM_001354523.2:c.*4A>G (UBE3A) | NP_001341452.1:n.*4A>G | |
| NM_001354538.2:c.*4A>G (UBE3A) | NP_001341467.1:n.*4A>G | |
| NM_001354539.2:c.*4A>G (UBE3A) | NP_001341468.1:n.*4A>G | |
| NM_001354540.2:c.*4A>G (UBE3A) | NP_001341469.1:n.*4A>G | |
| NM_001354541.2:c.*4A>G (UBE3A) | NP_001341470.1:n.*4A>G | |
| NM_001354542.2:c.*4A>G (UBE3A) | NP_001341471.1:n.*4A>G | |
| NM_001354543.2:c.*4A>G (UBE3A) | NP_001341472.1:n.*4A>G | |
| NM_001354544.2:c.*4A>G (UBE3A) | NP_001341473.1:n.*4A>G | |
| NM_001354545.2:c.*4A>G (UBE3A) | NP_001341474.1:n.*4A>G | |
| NM_001354546.2:c.*4A>G (UBE3A) | NP_001341475.1:n.*4A>G | |
| NM_001354547.2:c.*4A>G (UBE3A) | NP_001341476.1:n.*4A>G | |
| NM_001354548.2:c.*4A>G (UBE3A) | NP_001341477.1:n.*4A>G | |
| NM_001354549.2:c.*4A>G (UBE3A) | NP_001341478.1:n.*4A>G | |
| NM_001354550.2:c.*4A>G (UBE3A) | NP_001341479.1:n.*4A>G | |
| NM_001354551.2:c.*4A>G (UBE3A) | NP_001341480.1:n.*4A>G | |
| NM_001374461.1:c.*4A>G (UBE3A) | NP_001361390.1:n.*4A>G | |
| NM_130838.4:c.*4A>G (UBE3A) | NP_570853.1:n.*4A>G | |
| NM_130839.5:c.*4A>G (UBE3A) MANE Select | NP_570854.1:n.*4A>G | |
| NR_148916.2:n.3135A>G (UBE3A) |