Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97006253_97006261dup , CM000669.2:g.97006253_97006261dup | GRCh38 |
| NC_000007.13:g.96635565_96635573dup , CM000669.1:g.96635565_96635573dup | GRCh37 |
| NC_000007.12:g.96473501_96473509dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518156.3:c.276_284dup (DLX6) MANE Select | ENSP00000428480.2:p.His94_His95insGlnHisHis | |
| ENST00000518156.2:c.276_284dup (DLX6) | ENSP00000428480.2:p.His94_His95insGlnHisHis | |
| NM_005222.3:c.276_284dup (DLX6) | NP_005213.3:p.His94_His95insGlnHisHis | |
| NR_015448.1:n.141+7672_141+7680dup (DLX6-AS1) | ||
| NM_005222.4:c.276_284dup (DLX6) MANE Select | NP_005213.3:p.His94_His95insGlnHisHis |