| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97006103_97006105dup , CM000669.2:g.97006103_97006105dup | GRCh38 |
| NC_000007.13:g.96635415_96635417dup , CM000669.1:g.96635415_96635417dup | GRCh37 |
| NC_000007.12:g.96473351_96473353dup | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| NM_005222.4:c.126_128dup (DLX6) MANE Select | NP_005213.3:p.Gln43_Gln44insGln |
| ENST00000518156.3:c.126_128dup (DLX6) MANE Select | ENSP00000428480.2:p.Gln43_Gln44insGln |
| NM_005222.3:c.126_128dup (DLX6) | NP_005213.3:p.Gln43_Gln44insGln |
| NR_015448.1:n.141+7822_141+7824dup (DLX6-AS1) | |
| ENST00000518156.2:c.126_128dup (DLX6) | ENSP00000428480.2:p.Gln43_Gln44insGln |