Revel Score:
ENST00000370274 (MANE Select)
0.887
ENST00000440023
0.887
ENST00000432467
0.887
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.152865888G>A , CM000685.2:g.152865888G>A | GRCh38 |
| NC_000023.10:g.152034432G>A , CM000685.1:g.152034432G>A | GRCh37 |
| NC_000023.9:g.151785088G>A | NCBI36 |
| NG_009163.1:g.39922G>A | |
| NG_009163.2:g.39922G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370274.8:c.613G>A MANE Select | ENSP00000359297.3:p.Gly205Ser | |
| ENST00000370274.7:c.613G>A | ENSP00000359297.3:p.Gly205Ser | |
| ENST00000432467.1:c.613G>A | ENSP00000396266.1:p.Gly205Ser | |
| ENST00000440023.5:c.613G>A | ENSP00000391854.1:p.Gly205Ser | |
| NM_001129765.1:c.613G>A | NP_001123237.1:p.Gly205Ser | |
| NM_015922.2:c.613G>A | NP_057006.1:p.Gly205Ser | |
| XM_011531178.1:c.613G>A | XP_011529480.1:p.Gly205Ser | |
| XM_011531178.2:c.613G>A | XP_011529480.1:p.Gly205Ser | |
| XM_017029564.1:c.661G>A | XP_016885053.1:p.Gly221Ser | |
| NM_015922.3:c.613G>A MANE Select | NP_057006.1:p.Gly205Ser | |
| NM_001129765.2:c.613G>A | NP_001123237.1:p.Gly205Ser |