Revel Score:
ENST00000398092
0.921
ENST00000256682 (MANE Select)
0.921
ENST00000447318
0.921
ENST00000541959
0.921
ENST00000541236
0.921
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48939773A>G , CM000674.2:g.48939773A>G | GRCh38 |
| NC_000012.11:g.49333556A>G , CM000674.1:g.49333556A>G | GRCh37 |
| NC_000012.10:g.47619823A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256682.9:c.266T>C MANE Select | ENSP00000256682.4:p.Ile89Thr | |
| ENST00000256682.8:c.266T>C | ENSP00000256682.4:p.Ile89Thr | |
| ENST00000398092.4:c.266T>C | ENSP00000438507.1:p.Ile89Thr | |
| ENST00000447318.6:c.155T>C | ENSP00000395370.2:p.Ile52Thr | |
| ENST00000485410.5:n.137-926T>C | ||
| ENST00000541236.5:c.266T>C | ENSP00000438063.1:p.Ile89Thr | |
| ENST00000541959.5:c.266T>C | ENSP00000438510.1:p.Ile89Thr | |
| NM_001659.2:c.266T>C | NP_001650.1:p.Ile89Thr | |
| XM_005268856.1:c.266T>C | XP_005268913.1:p.Ile89Thr | |
| XM_006719391.2:c.266T>C | XP_006719454.1:p.Ile89Thr | |
| XM_011538322.1:c.266T>C | XP_011536624.1:p.Ile89Thr | |
| XM_011538323.1:c.266T>C | XP_011536625.1:p.Ile89Thr | |
| XM_006719391.4:c.266T>C | XP_006719454.1:p.Ile89Thr | |
| XM_024448972.1:c.266T>C | XP_024304740.1:p.Ile89Thr | |
| NM_001659.3:c.266T>C MANE Select | NP_001650.1:p.Ile89Thr |