Revel Score:
ENST00000311895 (MANE Select)
0.198
ENST00000389138
0.198
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13948138C>G , CM000678.2:g.13948138C>G | GRCh38 |
| NC_000016.9:g.14041995C>G , CM000678.1:g.14041995C>G | GRCh37 |
| NC_000016.8:g.13949496C>G | NCBI36 |
| NG_011442.1:g.32982C>G , LRG_463:g.32982C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2680C>G | ENSP00000507912.1:p.Pro894Ala | |
| ENST00000683962.1:c.*2236C>G | ENSP00000506854.1:n.*2236C>G | |
| ENST00000311895.8:c.2542C>G MANE Select | ENSP00000310520.7:p.Pro848Ala | |
| ENST00000311895.7:c.2542C>G | ENSP00000310520.7:p.Pro848Ala | |
| ENST00000389138.7:n.1819C>G | ||
| NM_005236.2:c.2542C>G , LRG_463t1:c.2542C>G | NP_005227.1:p.Pro848Ala | |
| XM_011522424.1:c.2680C>G | XP_011520726.1:p.Pro894Ala | |
| XM_011522425.1:c.1999C>G | XP_011520727.1:p.Pro667Ala | |
| XM_011522426.1:c.1753C>G | XP_011520728.1:p.Pro585Ala | |
| XM_011522427.1:c.1192C>G | XP_011520729.1:p.Pro398Ala | |
| XR_932805.1:n.2701C>G | ||
| XM_011522424.3:c.2680C>G | XP_011520726.1:p.Pro894Ala | |
| XM_017023043.2:c.1753C>G | XP_016878532.1:p.Pro585Ala | |
| NM_005236.3:c.2542C>G MANE Select | NP_005227.1:p.Pro848Ala |