Revel Score:
ENST00000435489
0.613
ENST00000311946 (MANE Select)
0.613
gnomAD v2:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157471785T>A , CM000667.2:g.157471785T>A | GRCh38 |
| NC_000005.9:g.156898793T>A , CM000667.1:g.156898793T>A | GRCh37 |
| NC_000005.8:g.156831371T>A | NCBI36 |
| NG_016626.1:g.16767T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311946.8:c.554T>A (NIPAL4) MANE Select | ENSP00000311687.8:p.Ile185Asn | |
| ENST00000435489.7:c.497T>A (NIPAL4) | ENSP00000406456.3:p.Ile166Asn | |
| ENST00000311946.7:c.740T>A (NIPAL4) | ENSP00000311687.7:p.Ile247Asn | |
| ENST00000435489.6:c.683T>A (NIPAL4) | ENSP00000406456.2:p.Ile228Asn | |
| ENST00000517951.5:c.*1741+16480A>T (ADAM19) | ENSP00000428376.1:n.*1741+16480A>T | |
| ENST00000519150.1:c.652T>A (NIPAL4) | ENSP00000430810.1:n.652T>A | |
| NM_001099287.1:c.740T>A (NIPAL4) | NP_001092757.1:p.Ile247Asn | |
| NM_001172292.1:c.683T>A (NIPAL4) | NP_001165763.1:p.Ile228Asn | |
| XM_011534552.1:c.245T>A (NIPAL4) | XP_011532854.1:p.Ile82Asn | |
| XM_024446043.1:c.41T>A (NIPAL4) | XP_024301811.1:p.Ile14Asn | |
| NM_001099287.2:c.554T>A (NIPAL4) MANE Select | NP_001092757.2:p.Ile185Asn |