Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97009915G>A , CM000669.2:g.97009915G>A | GRCh38 |
| NC_000007.13:g.96639227G>A , CM000669.1:g.96639227G>A | GRCh37 |
| NC_000007.12:g.96477163G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518156.3:c.750G>A (DLX6) MANE Select | ENSP00000428480.2:p.Ala250= | |
| ENST00000493273.2:n.1351G>A (DLX6) | ||
| ENST00000518156.2:c.750G>A (DLX6) | ENSP00000428480.2:p.Ala250= | |
| ENST00000555308.1:c.366G>A (DLX6) | ENSP00000451635.1:p.Ala122= | |
| NM_005222.3:c.750G>A (DLX6) | NP_005213.3:p.Ala250= | |
| NR_015448.1:n.141+4010C>T (DLX6-AS1) | ||
| NM_005222.4:c.750G>A (DLX6) MANE Select | NP_005213.3:p.Ala250= |