Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11845997T>C , CM000663.2:g.11845997T>C | GRCh38 |
| NC_000001.10:g.11906054T>C , CM000663.1:g.11906054T>C | GRCh37 |
| NC_000001.9:g.11828641T>C | NCBI36 |
| NG_012926.1:g.6787A>G , LRG_751:g.6787A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000400892.3:c.*1961+231T>C (CLCN6) | ENSP00000496938.1:n.*1961+231T>C | |
| ENST00000446542.5:n.781+231T>C (NPPA-AS1) | ||
| ENST00000376476.1:c.*12A>G (NPPA) | ENSP00000365659.1:n.*12A>G | |
| ENST00000376480.7:c.*12A>G (NPPA) MANE Select | ENSP00000365663.3:n.*12A>G | |
| ENST00000610706.1:c.*6A>G (NPPA) | ENSP00000483195.1:n.*6A>G | |
| NM_006172.3:c.*12A>G , LRG_751t1:c.*12A>G (NPPA) | NP_006163.1:n.*12A>G | |
| NR_037806.1:n.1479+231T>C (NPPA-AS1) | ||
| NM_006172.4:c.*12A>G (NPPA) MANE Select | NP_006163.1:n.*12A>G |