Revel Score:
ENST00000244709 (MANE Select)
0.016
ENST00000334475
0.016
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.41282727G>C , CM000668.2:g.41282727G>C | GRCh38 |
| NC_000006.11:g.41250465G>C , CM000668.1:g.41250465G>C | GRCh37 |
| NC_000006.10:g.41358443G>C | NCBI36 |
| NG_029525.1:g.8993C>G | |
| NG_029525.2:g.8993C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244709.9:c.74C>G MANE Select | ENSP00000244709.3:p.Thr25Ser | |
| ENST00000244709.8:c.74C>G | ENSP00000244709.3:p.Thr25Ser | |
| ENST00000334475.10:c.74C>G | ENSP00000334284.5:p.Thr25Ser | |
| ENST00000586287.1:n.101C>G | ||
| ENST00000589614.5:c.74C>G | ENSP00000465688.1:p.Thr25Ser | |
| ENST00000591620.1:c.74C>G | ENSP00000465345.1:p.Thr25Ser | |
| NM_001242589.1:c.74C>G | NP_001229518.1:p.Thr25Ser | |
| NM_001242590.1:c.74C>G | NP_001229519.1:p.Thr25Ser | |
| NM_018643.3:c.74C>G | NP_061113.1:p.Thr25Ser | |
| XM_006715117.2:c.74C>G | XP_006715180.1:p.Thr25Ser | |
| XM_011514696.1:c.74C>G | XP_011512998.1:p.Thr25Ser | |
| XM_011514697.1:c.74C>G | XP_011512999.1:p.Thr25Ser | |
| NM_001242589.2:c.74C>G | NP_001229518.1:p.Thr25Ser | |
| NM_001242590.2:c.74C>G | NP_001229519.1:p.Thr25Ser | |
| NM_018643.4:c.74C>G | NP_061113.1:p.Thr25Ser | |
| NR_136332.1:n.164C>G | ||
| XM_006715117.3:c.74C>G | XP_006715180.1:p.Thr25Ser | |
| XM_011514696.2:c.74C>G | XP_011512998.1:p.Thr25Ser | |
| XM_017010956.2:c.74C>G | XP_016866445.1:p.Thr25Ser | |
| XM_017010957.1:c.74C>G | XP_016866446.1:p.Thr25Ser | |
| NM_018643.5:c.74C>G MANE Select | NP_061113.1:p.Thr25Ser | |
| NM_001242589.3:c.74C>G | NP_001229518.1:p.Thr25Ser | |
| NM_001242590.3:c.74C>G | NP_001229519.1:p.Thr25Ser | |
| NR_136332.2:n.101C>G |