Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97006220_97006222dup , CM000669.2:g.97006220_97006222dup | GRCh38 |
| NC_000007.13:g.96635532_96635534dup , CM000669.1:g.96635532_96635534dup | GRCh37 |
| NC_000007.12:g.96473468_96473470dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005222.4:c.243_245dup (DLX6) MANE Select | NP_005213.3:p.Ala82_Ala83insAla |
| ENST00000518156.3:c.243_245dup (DLX6) MANE Select | ENSP00000428480.2:p.Ala82_Ala83insAla |
| NM_005222.3:c.243_245dup (DLX6) | NP_005213.3:p.Ala82_Ala83insAla |
| NR_015448.1:n.141+7705_141+7707dup (DLX6-AS1) | |
| ENST00000518156.2:c.243_245dup (DLX6) | ENSP00000428480.2:p.Ala82_Ala83insAla |