Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.47416336_47416339del , CM000663.2:g.47416336_47416339del | GRCh38 |
| NC_000001.10:g.47882008_47882011del , CM000663.1:g.47882008_47882011del | GRCh37 |
| NC_000001.9:g.47654595_47654598del | NCBI36 |
| NG_016192.1:g.5265_5268del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012186.3:c.21_24del (FOXE3) MANE Select | NP_036318.1:p.Met7IlefsTer? |
| ENST00000335071.4:c.21_24del (FOXE3) MANE Select | ENSP00000334472.2:p.Met7IlefsTer? |
| NM_012186.2:c.21_24del (FOXE3) | NP_036318.1:p.Met7IlefsTer? |
| NR_126355.1:n.29-6436_29-6433del (LINC01389) | |
| ENST00000335071.3:c.21_24del (FOXE3) | ENSP00000334472.2:p.Met7IlefsTer? |