Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.76140855G= , CM000679.2:g.76140855G= | GRCh38 |
| NC_000017.10:g.74136936G= , CM000679.1:g.74136936G= | GRCh37 |
| NC_000017.9:g.71648531G= | NCBI36 |
| NG_013345.1:g.5445C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001454.4:c.-170+259C= (FOXJ1) MANE Select | NP_001445.2:n.-170+259C= |
| ENST00000322957.7:c.-170+259C= (FOXJ1) MANE Select | ENSP00000323880.4:n.-170+259C= |
| NM_001454.3:c.-170+259C= (FOXJ1) | NP_001445.2:n.-170+259C= |
| NR_040017.1:n.125+175G= (RNF157-AS1) | |
| ENST00000322957.6:c.-170+259C= (FOXJ1) | ENSP00000323880.4:n.-170+259C= |