Revel Score:
ENST00000456935 (MANE Select)
0.428
ENST00000536796
0.428
ENST00000221363
0.428
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12661352T>A , CM000681.2:g.12661352T>A | GRCh38 |
| NC_000019.9:g.12772166T>A , CM000681.1:g.12772166T>A | GRCh37 |
| NC_000019.8:g.12633166T>A | NCBI36 |
| NG_008318.1:g.10426A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456935.7:c.934A>T MANE Select | ENSP00000395473.2:p.Thr312Ser | |
| ENST00000221363.8:c.934A>T | ENSP00000221363.4:p.Thr312Ser | |
| ENST00000456935.6:c.934A>T | ENSP00000395473.2:p.Thr312Ser | |
| ENST00000462144.1:n.127A>T | ||
| ENST00000466794.5:n.916A>T | ||
| NM_000528.3:c.934A>T | NP_000519.2:p.Thr312Ser | |
| NM_001173498.1:c.934A>T | NP_001166969.1:p.Thr312Ser | |
| XM_005259913.1:c.934A>T | XP_005259970.1:p.Thr312Ser | |
| XM_011528017.1:c.-85A>T | XP_011526319.1:n.-85A>T | |
| XM_005259913.2:c.934A>T | XP_005259970.1:p.Thr312Ser | |
| XM_024451518.1:c.-85A>T | XP_024307286.1:n.-85A>T | |
| NM_000528.4:c.934A>T MANE Select | NP_000519.2:p.Thr312Ser | |
| NM_001173498.2:c.934A>T | NP_001166969.1:p.Thr312Ser |