Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11847657T= , CM000663.2:g.11847657T= | GRCh38 |
| NC_000001.10:g.11907714T= , CM000663.1:g.11907714T= | GRCh37 |
| NC_000001.9:g.11830301T= | NCBI36 |
| NG_012926.1:g.5127A= , LRG_751:g.5127A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400892.3:c.*2042T= (CLCN6) | ENSP00000496938.1:n.*2042T= | |
| ENST00000446542.5:n.1005T= (NPPA-AS1) | ||
| ENST00000376476.1:c.-27-218A= (NPPA) | ENSP00000365659.1:n.-27-218A= | |
| ENST00000376480.7:c.28A= (NPPA) MANE Select | ENSP00000365663.3:p.Ser10= | |
| ENST00000610706.1:c.28A= (NPPA) | ENSP00000483195.1:p.Ser10= | |
| NM_006172.3:c.28A= , LRG_751t1:c.28A= (NPPA) | NP_006163.1:p.Ser10= | |
| NM_006172.4:c.28A= (NPPA) MANE Select | NP_006163.1:p.Ser10= |