Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97006126_97006137del , CM000669.2:g.97006126_97006137del | GRCh38 |
| NC_000007.13:g.96635438_96635449del , CM000669.1:g.96635438_96635449del | GRCh37 |
| NC_000007.12:g.96473374_96473385del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005222.4:c.149_160del (DLX6) MANE Select | NP_005213.3:p.Pro50_Pro53del |
| ENST00000518156.3:c.149_160del (DLX6) MANE Select | ENSP00000428480.2:p.Pro50_Pro53del |
| NM_005222.3:c.149_160del (DLX6) | NP_005213.3:p.Pro50_Pro53del |
| NR_015448.1:n.141+7805_141+7816del (DLX6-AS1) | |
| ENST00000518156.2:c.149_160del (DLX6) | ENSP00000428480.2:p.Pro50_Pro53del |