Revel Score:
ENST00000228841 (MANE Select)
0.683
ENST00000550439
0.683
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110915781T>C , CM000674.2:g.110915781T>C | GRCh38 |
| NC_000012.11:g.111353585T>C , CM000674.1:g.111353585T>C | GRCh37 |
| NC_000012.10:g.109837968T>C | NCBI36 |
| NG_007554.1:g.9797A>G , LRG_393:g.9797A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000228841.15:c.103A>G MANE Select | ENSP00000228841.8:p.Ile35Val | |
| ENST00000663220.1:c.46A>G | ENSP00000499568.1:p.Ile16Val | |
| ENST00000228841.12:c.103A>G | ENSP00000228841.7:p.Ile35Val | |
| ENST00000548438.1:c.94-1457A>G | ENSP00000447154.1:n.94-1457A>G | |
| NM_000432.3:c.103A>G , LRG_393t1:c.103A>G | NP_000423.2:p.Ile35Val | |
| NM_000432.4:c.103A>G MANE Select | NP_000423.2:p.Ile35Val |