Revel Score:
ENST00000324868 (MANE Select)
0.922
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.32755639C>A , CM000674.2:g.32755639C>A | GRCh38 |
| NC_000012.11:g.32908573C>A , CM000674.1:g.32908573C>A | GRCh37 |
| NC_000012.10:g.32799840C>A | NCBI36 |
| NG_028122.1:g.5315G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324868.13:c.236G>T MANE Select | ENSP00000320658.8:p.Gly79Val | |
| ENST00000324868.12:c.236G>T | ENSP00000320658.8:p.Gly79Val | |
| ENST00000548490.1:c.158G>T | ENSP00000447710.1:p.Gly53Val | |
| NM_001040436.2:c.236G>T | NP_001035526.1:p.Gly79Val | |
| XR_242891.3:n.323G>T | ||
| XR_242892.3:n.323G>T | ||
| XR_429036.1:n.323G>T | ||
| XR_931296.1:n.323G>T | ||
| XR_931297.1:n.323G>T | ||
| XR_931298.1:n.323G>T | ||
| XR_931299.1:n.323G>T | ||
| XR_001748730.2:n.820G>T | ||
| XR_002957331.1:n.820G>T | ||
| XR_242892.5:n.820G>T | ||
| XR_931296.3:n.820G>T | ||
| NM_001040436.3:c.236G>T MANE Select | NP_001035526.1:p.Gly79Val |