Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11846011A>T , CM000663.2:g.11846011A>T | GRCh38 |
| NC_000001.10:g.11906068A>T , CM000663.1:g.11906068A>T | GRCh37 |
| NC_000001.9:g.11828655A>T | NCBI36 |
| NG_012926.1:g.6773T>A , LRG_751:g.6773T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006172.4:c.454T>A (NPPA) MANE Select | NP_006163.1:p.Ter152Arg |
| ENST00000376480.7:c.454T>A (NPPA) MANE Select | ENSP00000365663.3:p.Ter152Arg |
| NM_006172.3:c.454T>A , LRG_751t1:c.454T>A (NPPA) | NP_006163.1:p.Ter152Arg |
| NR_037806.1:n.1479+245A>T (NPPA-AS1) | |
| ENST00000376476.1:c.304T>A (NPPA) | ENSP00000365659.1:p.Ter102Arg |
| ENST00000400892.3:c.*1961+245A>T (CLCN6) | ENSP00000496938.1:n.*1961+245A>T |
| ENST00000446542.5:n.781+245A>T (NPPA-AS1) | |
| ENST00000610706.1:c.453+1T>A (NPPA) | ENSP00000483195.1:n.453+1T>A |