Revel Score:
ENST00000324868 (MANE Select)
0.336
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.32747335T>G , CM000674.2:g.32747335T>G | GRCh38 |
| NC_000012.11:g.32900269T>G , CM000674.1:g.32900269T>G | GRCh37 |
| NC_000012.10:g.32791536T>G | NCBI36 |
| NG_012219.1:g.73133T>G | |
| NG_028122.1:g.13619A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324868.13:c.1303A>C MANE Select | ENSP00000320658.8:p.Ser435Arg | |
| ENST00000324868.12:c.1303A>C | ENSP00000320658.8:p.Ser435Arg | |
| ENST00000548490.1:c.1190A>C | ENSP00000447710.1:n.1190A>C | |
| ENST00000551673.5:n.200A>C | ||
| NM_001040436.2:c.1303A>C | NP_001035526.1:p.Ser435Arg | |
| XR_242891.3:n.1390A>C | ||
| XR_242892.3:n.1390A>C | ||
| XR_429036.1:n.1390A>C | ||
| XR_931296.1:n.1390A>C | ||
| XR_931297.1:n.1390A>C | ||
| XR_931298.1:n.1390A>C | ||
| XR_931299.1:n.1390A>C | ||
| XR_001748730.2:n.1887A>C | ||
| XR_002957331.1:n.1887A>C | ||
| XR_242892.5:n.1887A>C | ||
| XR_931296.3:n.1887A>C | ||
| NM_001040436.3:c.1303A>C MANE Select | NP_001035526.1:p.Ser435Arg |