Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11846007C>A , CM000663.2:g.11846007C>A | GRCh38 |
| NC_000001.10:g.11906064C>A , CM000663.1:g.11906064C>A | GRCh37 |
| NC_000001.9:g.11828651C>A | NCBI36 |
| NG_012926.1:g.6777G>T , LRG_751:g.6777G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006172.4:c.*2G>T (NPPA) MANE Select | NP_006163.1:n.*2G>T |
| ENST00000376480.7:c.*2G>T (NPPA) MANE Select | ENSP00000365663.3:n.*2G>T |
| NM_006172.3:c.*2G>T , LRG_751t1:c.*2G>T (NPPA) | NP_006163.1:n.*2G>T |
| NR_037806.1:n.1479+241C>A (NPPA-AS1) | |
| ENST00000376476.1:c.*2G>T (NPPA) | ENSP00000365659.1:n.*2G>T |
| ENST00000400892.3:c.*1961+241C>A (CLCN6) | ENSP00000496938.1:n.*1961+241C>A |
| ENST00000446542.5:n.781+241C>A (NPPA-AS1) | |
| ENST00000610706.1:c.455G>T (NPPA) | ENSP00000483195.1:p.Arg152Ile |