Revel Score:
ENST00000339994 (MANE Select)
0.834
ENST00000528731
0.834
ENST00000526912
0.834
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17387398G>T , CM000673.2:g.17387398G>T | GRCh38 |
| NC_000011.9:g.17408945G>T , CM000673.1:g.17408945G>T | GRCh37 |
| NC_000011.8:g.17365521G>T | NCBI36 |
| NG_012446.1:g.6262C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682350.1:c.433C>A | ENSP00000508090.1:p.Pro145Thr | |
| ENST00000682764.1:c.433C>A | ENSP00000506780.1:p.Pro145Thr | |
| ENST00000339994.5:c.694C>A MANE Select | ENSP00000345708.4:p.Pro232Thr | |
| ENST00000339994.4:c.694C>A | ENSP00000345708.4:p.Pro232Thr | |
| ENST00000526912.1:c.433C>A | ENSP00000432729.1:p.Pro145Thr | |
| ENST00000528731.1:c.433C>A | ENSP00000434755.1:p.Pro145Thr | |
| NM_000525.3:c.694C>A | NP_000516.3:p.Pro232Thr | |
| NM_001166290.1:c.433C>A | NP_001159762.1:p.Pro145Thr | |
| XM_006718226.2:c.433C>A | XP_006718289.1:p.Pro145Thr | |
| XR_930867.1:n.852C>A | ||
| XM_006718226.3:c.433C>A | XP_006718289.1:p.Pro145Thr | |
| XM_017017680.1:c.433C>A | XP_016873169.1:p.Pro145Thr | |
| NM_001166290.2:c.433C>A | NP_001159762.1:p.Pro145Thr | |
| NM_001377296.1:c.433C>A | NP_001364225.1:p.Pro145Thr | |
| NM_001377297.1:c.433C>A | NP_001364226.1:p.Pro145Thr | |
| NM_000525.4:c.694C>A MANE Select | NP_000516.3:p.Pro232Thr |