Revel Score:
ENST00000259523
0.064
ENST00000377970
0.064
ENST00000524013
0.064
ENST00000454617
0.064
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127738995C>G , CM000670.2:g.127738995C>G | GRCh38 |
| NC_000008.10:g.128751241C>G , CM000670.1:g.128751241C>G | GRCh37 |
| NC_000008.9:g.128820423C>G | NCBI36 |
| NG_007161.1:g.7926C>G | |
| NG_007161.2:g.8562C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000707113.1:c.733C>G | ENSP00000516742.1:p.Pro245Ala | |
| ENST00000707114.1:c.733C>G | ENSP00000516743.1:p.Pro245Ala | |
| ENST00000707115.1:c.733C>G | ENSP00000516744.1:p.Pro245Ala | |
| ENST00000707116.1:c.733C>G | ENSP00000516745.1:p.Pro245Ala | |
| ENST00000524013.2:c.775C>G | ENSP00000430235.2:p.Pro259Ala | |
| ENST00000621592.8:c.778C>G MANE Select | ENSP00000478887.2:p.Pro260Ala | |
| ENST00000651626.1:c.433C>G | ENSP00000499182.1:p.Pro145Ala | |
| ENST00000652288.1:c.733C>G | ENSP00000499105.1:p.Pro245Ala | |
| ENST00000259523.10:c.733C>G | ENSP00000259523.6:p.Pro245Ala | |
| ENST00000377970.6:c.733C>G | ENSP00000367207.3:p.Pro245Ala | |
| ENST00000524013.1:c.775C>G | ENSP00000430235.1:p.Pro259Ala | |
| ENST00000613283.1:c.778C>G | ENSP00000479618.1:p.Pro260Ala | |
| ENST00000621592.5:c.778C>G | ENSP00000478887.1:p.Pro260Ala | |
| NM_002467.4:c.778C>G | NP_002458.2:p.Pro260Ala | |
| NM_001354870.1:c.775C>G | NP_001341799.1:p.Pro259Ala | |
| NM_002467.5:c.778C>G | NP_002458.2:p.Pro260Ala | |
| NM_002467.6:c.778C>G MANE Select | NP_002458.2:p.Pro260Ala |