| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965612_37965613del , CM000670.2:g.37965612_37965613del | GRCh38 |
| NC_000008.10:g.37823130_37823131del , CM000670.1:g.37823130_37823131del | GRCh37 |
| NC_000008.9:g.37942287_37942288del | NCBI36 |
| NG_011936.1:g.6055_6056del |
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.858_859del MANE Select | NP_000016.1:p.Glu287ThrfsTer? |
| ENST00000345060.5:c.858_859del MANE Select | ENSP00000343782.3:p.Glu287ThrfsTer? |
| NM_000025.2:c.858_859del | NP_000016.1:p.Glu287ThrfsTer? |
| ENST00000345060.4:c.858_859del | ENSP00000343782.3:p.Glu287ThrfsTer? |
| ENST00000520341.1:n.133_134del | |
| ENST00000520341.2:n.986_987del | |
| ENST00000614635.1:c.858_859del | ENSP00000480325.1:p.Glu287ThrfsTer? |
| ENST00000647937.1:c.342_343del | ENSP00000497740.1:p.Glu115ThrfsTer? |