| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965618_37965619del , CM000670.2:g.37965618_37965619del | GRCh38 |
| NC_000008.10:g.37823136_37823137del , CM000670.1:g.37823136_37823137del | GRCh37 |
| NC_000008.9:g.37942293_37942294del | NCBI36 |
| NG_011936.1:g.6051_6052del |
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.854_855del MANE Select | NP_000016.1:p.Leu285ProfsTer? |
| ENST00000345060.5:c.854_855del MANE Select | ENSP00000343782.3:p.Leu285ProfsTer? |
| NM_000025.2:c.854_855del | NP_000016.1:p.Leu285ProfsTer? |
| ENST00000345060.4:c.854_855del | ENSP00000343782.3:p.Leu285ProfsTer? |
| ENST00000520341.1:n.129_130del | |
| ENST00000520341.2:n.982_983del | |
| ENST00000614635.1:c.854_855del | ENSP00000480325.1:p.Leu285ProfsTer? |
| ENST00000647937.1:c.338_339del | ENSP00000497740.1:p.Leu113ProfsTer? |