Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97010011A>G , CM000669.2:g.97010011A>G | GRCh38 |
| NC_000007.13:g.96639323A>G , CM000669.1:g.96639323A>G | GRCh37 |
| NC_000007.12:g.96477259A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518156.3:c.846A>G (DLX6) MANE Select | ENSP00000428480.2:p.Pro282= | |
| ENST00000493273.2:n.1447A>G (DLX6) | ||
| ENST00000518156.2:c.846A>G (DLX6) | ENSP00000428480.2:p.Pro282= | |
| ENST00000555308.1:c.462A>G (DLX6) | ENSP00000451635.1:p.Pro154= | |
| NM_005222.3:c.846A>G (DLX6) | NP_005213.3:p.Pro282= | |
| NR_015448.1:n.141+3914T>C (DLX6-AS1) | ||
| NM_005222.4:c.846A>G (DLX6) MANE Select | NP_005213.3:p.Pro282= |