Revel Score:
ENST00000326873 (MANE Select)
0.472
ENST00000405031
0.472
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1221963G>C , CM000681.2:g.1221963G>C | GRCh38 |
| NC_000019.9:g.1221962G>C , CM000681.1:g.1221962G>C | GRCh37 |
| NC_000019.8:g.1172962G>C | NCBI36 |
| NG_007460.2:g.37557G>C , LRG_319:g.37557G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.877G>C | ENSP00000490268.2:p.Glu293Gln | |
| ENST00000585748.3:c.505G>C | ENSP00000477641.2:p.Glu169Gln | |
| ENST00000585851.2:c.703G>C | ENSP00000467912.2:p.Glu235Gln | |
| ENST00000326873.12:c.877G>C MANE Select | ENSP00000324856.6:p.Glu293Gln | |
| ENST00000652231.1:c.877G>C | ENSP00000498804.1:p.Glu293Gln | |
| ENST00000326873.11:c.877G>C | ENSP00000324856.6:p.Glu293Gln | |
| ENST00000586243.5:c.877G>C | ENSP00000467240.2:p.Glu293Gln | |
| ENST00000589152.5:n.1575G>C | ||
| ENST00000591133.2:n.848G>C | ||
| NM_000455.4:c.877G>C , LRG_319t1:c.877G>C | NP_000446.1:p.Glu293Gln | |
| XM_005259617.1:c.877G>C | XP_005259674.1:p.Glu293Gln | |
| XM_005259618.3:c.877G>C | XP_005259675.1:p.Glu293Gln | |
| XM_011528209.1:c.655G>C | XP_011526511.1:p.Glu219Gln | |
| XR_936204.1:n.1653G>C | ||
| XM_005259617.3:c.877G>C | XP_005259674.1:p.Glu293Gln | |
| XM_011528209.2:c.655G>C | XP_011526511.1:p.Glu219Gln | |
| XR_001753738.2:n.1683G>C | ||
| XR_001753739.1:n.1683G>C | ||
| XR_001753740.2:n.1653G>C | ||
| NM_000455.5:c.877G>C MANE Select | NP_000446.1:p.Glu293Gln |