Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.47417247_47417259del , CM000663.2:g.47417247_47417259del | GRCh38 |
| NC_000001.10:g.47882919_47882931del , CM000663.1:g.47882919_47882931del | GRCh37 |
| NC_000001.9:g.47655506_47655518del | NCBI36 |
| NG_016192.1:g.6176_6188del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012186.3:c.932_944del (FOXE3) MANE Select | NP_036318.1:p.Phe311TrpfsTer? |
| ENST00000335071.4:c.932_944del (FOXE3) MANE Select | ENSP00000334472.2:p.Phe311TrpfsTer? |
| NM_012186.2:c.932_944del (FOXE3) | NP_036318.1:p.Phe311TrpfsTer? |
| NR_126355.1:n.29-7353_29-7341del (LINC01389) | |
| ENST00000335071.3:c.932_944del (FOXE3) | ENSP00000334472.2:p.Phe311TrpfsTer? |