Revel Score:
ENST00000545199
0.018
ENST00000539261 (MANE Select)
0.019
ENST00000228938
0.019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14882146G>C , CM000674.2:g.14882146G>C | GRCh38 |
| NC_000012.11:g.15035080G>C , CM000674.1:g.15035080G>C | GRCh37 |
| NC_000012.10:g.14926347G>C | NCBI36 |
| NG_023331.1:g.8774C>G | |
| NG_023331.2:g.8774C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539261.6:c.305C>G (MGP) MANE Select | ENSP00000445907.1:p.Thr102Ser | |
| ENST00000648334.1:n.126-21861G>C (C12orf60) | ||
| ENST00000228938.5:c.380C>G (MGP) | ENSP00000228938.5:p.Thr127Ser | |
| ENST00000527783.1:n.76-17023G>C (C12orf60) | ||
| ENST00000533472.1:n.87-21861G>C (C12orf60) | ||
| ENST00000539261.5:c.305C>G (MGP) | ENSP00000445907.1:p.Thr102Ser | |
| ENST00000545199.5:c.168C>G (MGP) | ||
| NM_000900.3:c.305C>G (MGP) | NP_000891.2:p.Thr102Ser | |
| NM_001190839.1:c.380C>G (MGP) | NP_001177768.1:p.Thr127Ser | |
| NM_000900.4:c.305C>G (MGP) | NP_000891.2:p.Thr102Ser | |
| NM_001190839.2:c.380C>G (MGP) | NP_001177768.1:p.Thr127Ser | |
| NM_000900.5:c.305C>G (MGP) MANE Select | NP_000891.2:p.Thr102Ser | |
| NM_001190839.3:c.380C>G (MGP) | NP_001177768.1:p.Thr127Ser |