Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11847373T= , CM000663.2:g.11847373T= | GRCh38 |
| NC_000001.10:g.11907430T= , CM000663.1:g.11907430T= | GRCh37 |
| NC_000001.9:g.11830017T= | NCBI36 |
| NG_012926.1:g.5411A= , LRG_751:g.5411A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006172.4:c.190A= (NPPA) MANE Select | NP_006163.1:p.Ser64= |
| ENST00000376480.7:c.190A= (NPPA) MANE Select | ENSP00000365663.3:p.Ser64= |
| NM_006172.3:c.190A= , LRG_751t1:c.190A= (NPPA) | NP_006163.1:p.Ser64= |
| NR_037806.1:n.1480-61T= (NPPA-AS1) | |
| ENST00000376476.1:c.40A= (NPPA) | ENSP00000365659.1:p.Ser14= |
| ENST00000400892.3:c.*1962-204T= (CLCN6) | ENSP00000496938.1:n.*1962-204T= |
| ENST00000446542.5:n.782-61T= (NPPA-AS1) | |
| ENST00000610706.1:c.190A= (NPPA) | ENSP00000483195.1:p.Ser64= |