Revel Score:
ENST00000435489
0.291
ENST00000311946 (MANE Select)
0.291
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157471788T>G , CM000667.2:g.157471788T>G | GRCh38 |
| NC_000005.9:g.156898796T>G , CM000667.1:g.156898796T>G | GRCh37 |
| NC_000005.8:g.156831374T>G | NCBI36 |
| NG_016626.1:g.16770T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311946.8:c.557T>G (NIPAL4) MANE Select | ENSP00000311687.8:p.Met186Arg | |
| ENST00000435489.7:c.500T>G (NIPAL4) | ENSP00000406456.3:p.Met167Arg | |
| ENST00000311946.7:c.743T>G (NIPAL4) | ENSP00000311687.7:p.Met248Arg | |
| ENST00000435489.6:c.686T>G (NIPAL4) | ENSP00000406456.2:p.Met229Arg | |
| ENST00000517951.5:c.*1741+16477A>C (ADAM19) | ENSP00000428376.1:n.*1741+16477A>C | |
| ENST00000519150.1:c.655T>G (NIPAL4) | ENSP00000430810.1:n.655T>G | |
| NM_001099287.1:c.743T>G (NIPAL4) | NP_001092757.1:p.Met248Arg | |
| NM_001172292.1:c.686T>G (NIPAL4) | NP_001165763.1:p.Met229Arg | |
| XM_011534552.1:c.248T>G (NIPAL4) | XP_011532854.1:p.Met83Arg | |
| XM_024446043.1:c.44T>G (NIPAL4) | XP_024301811.1:p.Met15Arg | |
| NM_001099287.2:c.557T>G (NIPAL4) MANE Select | NP_001092757.2:p.Met186Arg |