Revel Score:
ENST00000426263 (MANE Select)
0.878
ENST00000372501
0.878
ENST00000397019
0.878
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.42927726A>C , CM000663.2:g.42927726A>C | GRCh38 |
| NC_000001.10:g.43393397A>C , CM000663.1:g.43393397A>C | GRCh37 |
| NC_000001.9:g.43165984A>C | NCBI36 |
| NG_008232.1:g.36451T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426263.10:c.1157T>G MANE Select | ENSP00000416293.2:p.Ile386Ser | |
| ENST00000674545.1:n.1774T>G | ||
| ENST00000674765.1:c.1030-869T>G | ENSP00000501811.1:n.1030-869T>G | |
| ENST00000675112.1:n.1458T>G | ||
| ENST00000676254.1:n.1606T>G | ||
| ENST00000426263.7:c.1157T>G | ENSP00000416293.2:p.Ile386Ser | |
| ENST00000475162.3:c.416-748T>G | ||
| ENST00000630287.2:c.*472T>G | ENSP00000486694.1:n.*472T>G | |
| NM_006516.2:c.1157T>G | NP_006507.2:p.Ile386Ser | |
| NM_006516.3:c.1157T>G | NP_006507.2:p.Ile386Ser | |
| NM_006516.4:c.1157T>G MANE Select | NP_006507.2:p.Ile386Ser |