| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965632_37965633del , CM000670.2:g.37965632_37965633del | GRCh38 |
| NC_000008.10:g.37823150_37823151del , CM000670.1:g.37823150_37823151del | GRCh37 |
| NC_000008.9:g.37942307_37942308del | NCBI36 |
| NG_011936.1:g.6039_6040del |
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.842_843del MANE Select | NP_000016.1:p.Arg281ProfsTer? |
| ENST00000345060.5:c.842_843del MANE Select | ENSP00000343782.3:p.Arg281ProfsTer? |
| NM_000025.2:c.842_843del | NP_000016.1:p.Arg281ProfsTer? |
| ENST00000345060.4:c.842_843del | ENSP00000343782.3:p.Arg281ProfsTer? |
| ENST00000520341.1:n.117_118del | |
| ENST00000520341.2:n.970_971del | |
| ENST00000614635.1:c.842_843del | ENSP00000480325.1:p.Arg281ProfsTer? |
| ENST00000647937.1:c.326_327del | ENSP00000497740.1:p.Arg109ProfsTer? |