Revel Score:
ENST00000252490 (MANE Select)
0.139
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44948485A>G , CM000681.2:g.44948485A>G | GRCh38 |
| NC_000019.9:g.45451742A>G , CM000681.1:g.45451742A>G | GRCh37 |
| NC_000019.8:g.50143582A>G | NCBI36 |
| NG_008837.1:g.7500A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252490.7:c.7A>G (APOC2) MANE Select | ENSP00000252490.5:p.Thr3Ala | |
| ENST00000252490.5:c.7A>G (APOC4-APOC2) | ENSP00000252490.4:p.Thr3Ala | |
| ENST00000585685.5:c.*790A>G (APOC4-APOC2) | ENSP00000467185.1:n.*790A>G | |
| ENST00000585786.1:c.7A>G (APOC2) | ENSP00000465001.1:p.Thr3Ala | |
| ENST00000589057.5:c.238A>G (APOC4-APOC2) | ENSP00000468139.1:p.Thr80Ala | |
| ENST00000590360.2:c.7A>G (APOC2) | ENSP00000466775.1:p.Thr3Ala | |
| ENST00000591597.5:c.7A>G (APOC2) | ENSP00000476835.1:p.Thr3Ala | |
| ENST00000592257.5:c.7A>G (APOC2) | ENSP00000477261.1:p.Thr3Ala | |
| NM_000483.4:c.7A>G (APOC2) | NP_000474.2:p.Thr3Ala | |
| NR_037932.1:n.1214A>G (APOC4-APOC2) | ||
| NM_000483.5:c.7A>G (APOC2) MANE Select | NP_000474.2:p.Thr3Ala |