Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6999441A>T , CM000679.2:g.6999441A>T | GRCh38 |
| NC_000017.10:g.6902760A>T , CM000679.1:g.6902760A>T | GRCh37 |
| NC_000017.9:g.6843484A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000697.3:c.782A>T (ALOX12) MANE Select | NP_000688.2:p.Gln261Leu |
| ENST00000251535.11:c.782A>T (ALOX12) MANE Select | ENSP00000251535.6:p.Gln261Leu |
| NM_000697.2:c.782A>T (ALOX12) | NP_000688.2:p.Gln261Leu |
| NR_040089.1:n.233+10355T>A (ALOX12-AS1) | |
| ENST00000251535.10:c.782A>T (ALOX12) | ENSP00000251535.6:p.Gln261Leu |
| ENST00000480801.1:c.284A>T (ALOX12) | ENSP00000467033.1:p.Gln95Leu |
| XM_011523780.1:c.932A>T (ALOX12) | XP_011522082.1:p.Gln311Leu |
| XM_011523780.2:c.932A>T (ALOX12) | XP_011522082.1:p.Gln311Leu |