Revel Score:
ENST00000435489
0.829
ENST00000311946 (MANE Select)
0.829
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157471691C>A , CM000667.2:g.157471691C>A | GRCh38 |
| NC_000005.9:g.156898699C>A , CM000667.1:g.156898699C>A | GRCh37 |
| NC_000005.8:g.156831277C>A | NCBI36 |
| NG_016626.1:g.16673C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311946.8:c.460C>A (NIPAL4) MANE Select | ENSP00000311687.8:p.Leu154Met | |
| ENST00000435489.7:c.403C>A (NIPAL4) | ENSP00000406456.3:p.Leu135Met | |
| ENST00000311946.7:c.646C>A (NIPAL4) | ENSP00000311687.7:p.Leu216Met | |
| ENST00000435489.6:c.589C>A (NIPAL4) | ENSP00000406456.2:p.Leu197Met | |
| ENST00000517951.5:c.*1741+16574G>T (ADAM19) | ENSP00000428376.1:n.*1741+16574G>T | |
| ENST00000519150.1:c.558C>A (NIPAL4) | ENSP00000430810.1:n.558C>A | |
| NM_001099287.1:c.646C>A (NIPAL4) | NP_001092757.1:p.Leu216Met | |
| NM_001172292.1:c.589C>A (NIPAL4) | NP_001165763.1:p.Leu197Met | |
| XM_011534552.1:c.151C>A (NIPAL4) | XP_011532854.1:p.Leu51Met | |
| XM_024446043.1:c.-54C>A (NIPAL4) | XP_024301811.1:n.-54C>A | |
| NM_001099287.2:c.460C>A (NIPAL4) MANE Select | NP_001092757.2:p.Leu154Met |