dbSNP:
gnomAD v4:
Revel Score:
ENST00000435489
0.330
ENST00000311946 (MANE Select)
0.330
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157471682A>T , CM000667.2:g.157471682A>T | GRCh38 |
| NC_000005.9:g.156898690A>T , CM000667.1:g.156898690A>T | GRCh37 |
| NC_000005.8:g.156831268A>T | NCBI36 |
| NG_016626.1:g.16664A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311946.8:c.451A>T (NIPAL4) MANE Select | ENSP00000311687.8:p.Arg151Trp | |
| ENST00000435489.7:c.394A>T (NIPAL4) | ENSP00000406456.3:p.Arg132Trp | |
| ENST00000311946.7:c.637A>T (NIPAL4) | ENSP00000311687.7:p.Arg213Trp | |
| ENST00000435489.6:c.580A>T (NIPAL4) | ENSP00000406456.2:p.Arg194Trp | |
| ENST00000517951.5:c.*1741+16583T>A (ADAM19) | ENSP00000428376.1:n.*1741+16583T>A | |
| ENST00000519150.1:c.549A>T (NIPAL4) | ENSP00000430810.1:n.549A>T | |
| NM_001099287.1:c.637A>T (NIPAL4) | NP_001092757.1:p.Arg213Trp | |
| NM_001172292.1:c.580A>T (NIPAL4) | NP_001165763.1:p.Arg194Trp | |
| XM_011534552.1:c.142A>T (NIPAL4) | XP_011532854.1:p.Arg48Trp | |
| XM_024446043.1:c.-63A>T (NIPAL4) | XP_024301811.1:n.-63A>T | |
| NM_001099287.2:c.451A>T (NIPAL4) MANE Select | NP_001092757.2:p.Arg151Trp |