Revel Score:
ENST00000357249
0.286
ENST00000359125 (MANE Select)
0.286
ENST00000370226
0.286
ENST00000354587
0.286
ENST00000359689
0.286
ENST00000430658
0.286
ENST00000360480
0.286
ENST00000344462
0.286
ENST00000370224
0.286
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63408487T>A , CM000682.2:g.63408487T>A | GRCh38 |
| NC_000020.10:g.62039840T>A , CM000682.1:g.62039840T>A | GRCh37 |
| NC_000020.9:g.61510284T>A | NCBI36 |
| NG_009004.1:g.69154A>T | |
| NG_009004.2:g.69154A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706989.1:c.1867A>T | ENSP00000516702.1:p.Thr623Ser | |
| ENST00000359125.7:c.1813A>T MANE Select | ENSP00000352035.2:p.Thr605Ser | |
| ENST00000636614.1:c.139A>T | ||
| ENST00000637193.1:c.1210A>T | ENSP00000490734.1:p.Thr404Ser | |
| ENST00000344462.8:c.1720A>T | ENSP00000339611.4:p.Thr574Ser | |
| ENST00000357249.6:c.1381A>T | ENSP00000349789.3:p.Thr461Ser | |
| ENST00000359125.6:c.1813A>T | ENSP00000352035.2:p.Thr605Ser | |
| ENST00000360480.7:c.1729A>T | ENSP00000353668.3:p.Thr577Ser | |
| ENST00000370224.5:c.1837A>T | ENSP00000359244.2:p.Thr613Ser | |
| ENST00000625514.2:c.1801A>T | ENSP00000486040.1:p.Thr601Ser | |
| ENST00000626839.2:c.1759A>T | ENSP00000486706.1:p.Thr587Ser | |
| ENST00000629241.2:c.1729A>T | ENSP00000487142.1:p.Thr577Ser | |
| ENST00000629676.2:c.1679+4963A>T | ENSP00000486194.1:n.1679+4963A>T | |
| NM_004518.4:c.1729A>T | NP_004509.2:p.Thr577Ser | |
| NM_172106.1:c.1759A>T | NP_742104.1:p.Thr587Ser | |
| NM_172107.2:c.1813A>T | NP_742105.1:p.Thr605Ser | |
| NM_172108.3:c.1720A>T | NP_742106.1:p.Thr574Ser | |
| XM_006723787.1:c.1855A>T | XP_006723850.1:p.Thr619Ser | |
| XM_011528807.1:c.1921A>T | XP_011527109.1:p.Thr641Ser | |
| XM_011528808.1:c.1918A>T | XP_011527110.1:p.Thr640Ser | |
| XM_011528809.1:c.1891A>T | XP_011527111.1:p.Thr631Ser | |
| XM_011528810.1:c.1867A>T | XP_011527112.1:p.Thr623Ser | |
| XM_011528811.1:c.1837A>T | XP_011527113.1:p.Thr613Ser | |
| XM_011528812.1:c.1810A>T | XP_011527114.1:p.Thr604Ser | |
| XM_011528813.1:c.1795A>T | XP_011527115.1:p.Thr599Ser | |
| XM_011528814.1:c.1402A>T | XP_011527116.1:p.Thr468Ser | |
| XM_011528815.1:c.1921A>T | XP_011527117.1:p.Thr641Ser | |
| NM_004518.5:c.1729A>T | NP_004509.2:p.Thr577Ser | |
| NM_172106.2:c.1759A>T | NP_742104.1:p.Thr587Ser | |
| NM_172107.3:c.1813A>T | NP_742105.1:p.Thr605Ser | |
| NM_172108.4:c.1720A>T | NP_742106.1:p.Thr574Ser | |
| XM_011528810.2:c.1867A>T | XP_011527112.1:p.Thr623Ser | |
| XM_011528811.2:c.1837A>T | XP_011527113.1:p.Thr613Ser | |
| XM_017027841.2:c.1864A>T | XP_016883330.1:p.Thr622Ser | |
| XM_017027842.2:c.1801A>T | XP_016883331.1:p.Thr601Ser | |
| XM_017027843.1:c.1798A>T | XP_016883332.1:p.Thr600Ser | |
| XM_017027844.2:c.1756A>T | XP_016883333.1:p.Thr586Ser | |
| XM_017027845.1:c.829A>T | XP_016883334.1:p.Thr277Ser | |
| NM_004518.6:c.1729A>T | NP_004509.2:p.Thr577Ser | |
| NM_172106.3:c.1759A>T | NP_742104.1:p.Thr587Ser | |
| NM_172107.4:c.1813A>T MANE Select | NP_742105.1:p.Thr605Ser | |
| NM_172108.5:c.1720A>T | NP_742106.1:p.Thr574Ser | |
| NM_001382235.1:c.1867A>T | NP_001369164.1:p.Thr623Ser |