Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.43958588C>A , CM000685.2:g.43958588C>A | GRCh38 |
| NC_000023.10:g.43817834C>A , CM000685.1:g.43817834C>A | GRCh37 |
| NC_000023.9:g.43702778C>A | NCBI36 |
| NG_009832.1:g.20088G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000266.4:c.58G>T (NDP) MANE Select | NP_000257.1:p.Gly20Ter |
| ENST00000642620.1:c.58G>T (NDP) MANE Select | ENSP00000495972.1:p.Gly20Ter |
| NM_000266.3:c.58G>T (NDP) | NP_000257.1:p.Gly20Ter |
| NR_046631.1:n.467-2197C>A (NDP-AS1) | |
| ENST00000378062.5:c.58G>T (NDP) | ENSP00000367301.5:p.Gly20Ter |
| ENST00000470584.1:n.218+130G>T (NDP) | |
| ENST00000647044.1:c.58G>T (NDP) | ENSP00000495811.1:p.Gly20Ter |