Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97009914C>T , CM000669.2:g.97009914C>T | GRCh38 |
| NC_000007.13:g.96639226C>T , CM000669.1:g.96639226C>T | GRCh37 |
| NC_000007.12:g.96477162C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518156.3:c.749C>T (DLX6) MANE Select | ENSP00000428480.2:p.Ala250Val | |
| ENST00000493273.2:n.1350C>T (DLX6) | ||
| ENST00000518156.2:c.749C>T (DLX6) | ENSP00000428480.2:p.Ala250Val | |
| ENST00000555308.1:c.365C>T (DLX6) | ENSP00000451635.1:p.Ala122Val | |
| NM_005222.3:c.749C>T (DLX6) | NP_005213.3:p.Ala250Val | |
| NR_015448.1:n.141+4011G>A (DLX6-AS1) | ||
| NM_005222.4:c.749C>T (DLX6) MANE Select | NP_005213.3:p.Ala250Val |