Revel Score:
ENST00000360184 (MANE Select)
0.499
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102027662C>T , CM000676.2:g.102027662C>T | GRCh38 |
| NC_000014.8:g.102493999C>T , CM000676.1:g.102493999C>T | GRCh37 |
| NC_000014.7:g.101563752C>T | NCBI36 |
| NG_008777.1:g.68135C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684561.1:c.*551C>T | ENSP00000506816.1:n.*551C>T | |
| ENST00000360184.10:c.9092C>T MANE Select | ENSP00000348965.4:p.Thr3031Met | |
| ENST00000643508.2:c.9092C>T | ENSP00000495528.2:p.Thr3031Met | |
| ENST00000644881.2:c.9092C>T | ENSP00000495022.2:p.Thr3031Met | |
| ENST00000645039.2:c.9092C>T | ENSP00000495220.2:p.Thr3031Met | |
| ENST00000645149.2:c.9092C>T | ENSP00000495944.2:p.Thr3031Met | |
| ENST00000647366.1:n.2646C>T | ||
| ENST00000679486.1:c.9092C>T | ENSP00000506688.1:p.Thr3031Met | |
| ENST00000679629.1:c.9092C>T | ENSP00000505589.1:p.Thr3031Met | |
| ENST00000679720.1:c.9092C>T | ENSP00000505938.1:p.Thr3031Met | |
| ENST00000679910.1:c.*174C>T | ENSP00000506521.1:n.*174C>T | |
| ENST00000680120.1:c.9092C>T | ENSP00000504863.1:p.Thr3031Met | |
| ENST00000680137.1:c.9092C>T | ENSP00000505294.1:p.Thr3031Met | |
| ENST00000680200.1:c.9092C>T | ENSP00000506166.1:p.Thr3031Met | |
| ENST00000680313.1:c.9092C>T | ENSP00000506208.1:p.Thr3031Met | |
| ENST00000680423.1:c.*823C>T | ENSP00000505483.1:n.*823C>T | |
| ENST00000680715.1:c.9092C>T | ENSP00000505332.1:p.Thr3031Met | |
| ENST00000680808.1:c.*151C>T | ENSP00000506446.1:n.*151C>T | |
| ENST00000680874.1:c.9092C>T | ENSP00000504911.1:p.Thr3031Met | |
| ENST00000681010.1:c.9092C>T | ENSP00000505201.1:p.Thr3031Met | |
| ENST00000681066.1:c.9092C>T | ENSP00000506344.1:p.Thr3031Met | |
| ENST00000681123.1:c.9092C>T | ENSP00000506124.1:p.Thr3031Met | |
| ENST00000681283.1:c.9092C>T | ENSP00000505667.1:p.Thr3031Met | |
| ENST00000681311.1:c.*565C>T | ENSP00000505519.1:n.*565C>T | |
| ENST00000681536.1:c.*2291C>T | ENSP00000505821.1:n.*2291C>T | |
| ENST00000681574.1:c.9092C>T | ENSP00000505523.1:p.Thr3031Met | |
| ENST00000681822.1:c.9092C>T | ENSP00000505744.1:p.Thr3031Met | |
| ENST00000360184.8:c.9092C>T | ENSP00000348965.4:p.Thr3031Met | |
| ENST00000554854.1:n.156C>T | ||
| NM_001376.4:c.9092C>T | NP_001367.2:p.Thr3031Met | |
| NM_001376.5:c.9092C>T MANE Select | NP_001367.2:p.Thr3031Met |