Revel Score:
ENST00000320868 (MANE Select)
0.802
ENST00000397797
0.802
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177313G>A , CM000678.2:g.177313G>A | GRCh38 |
| NC_000016.9:g.227312G>A , CM000678.1:g.227312G>A | GRCh37 |
| NC_000016.8:g.167312G>A | NCBI36 |
| NG_000006.1:g.38176G>A | |
| NG_059186.1:g.5663G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.331G>A MANE Select | ENSP00000322421.5:p.Ala111Thr | |
| ENST00000397797.1:c.235G>A | ENSP00000380899.1:p.Ala79Thr | |
| ENST00000472694.1:n.467G>A | ||
| NM_000558.4:c.331G>A | NP_000549.1:p.Ala111Thr | |
| NM_000558.5:c.331G>A MANE Select | NP_000549.1:p.Ala111Thr |