Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11847392G>A , CM000663.2:g.11847392G>A | GRCh38 |
| NC_000001.10:g.11907449G>A , CM000663.1:g.11907449G>A | GRCh37 |
| NC_000001.9:g.11830036G>A | NCBI36 |
| NG_012926.1:g.5392C>T , LRG_751:g.5392C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006172.4:c.171C>T (NPPA) MANE Select | NP_006163.1:p.Val57= |
| ENST00000376480.7:c.171C>T (NPPA) MANE Select | ENSP00000365663.3:p.Val57= |
| NM_006172.3:c.171C>T , LRG_751t1:c.171C>T (NPPA) | NP_006163.1:p.Val57= |
| NR_037806.1:n.1480-42G>A (NPPA-AS1) | |
| ENST00000376476.1:c.21C>T (NPPA) | ENSP00000365659.1:p.Val7= |
| ENST00000400892.3:c.*1962-185G>A (CLCN6) | ENSP00000496938.1:n.*1962-185G>A |
| ENST00000446542.5:n.782-42G>A (NPPA-AS1) | |
| ENST00000610706.1:c.171C>T (NPPA) | ENSP00000483195.1:p.Val57= |