| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176759_176761delinsCGA , CM000678.2:g.176759_176761delinsCGA | GRCh38 |
| NC_000016.9:g.226758_226760delinsCGA , CM000678.1:g.226758_226760delinsCGA | GRCh37 |
| NC_000016.8:g.166758_166760delinsCGA | NCBI36 |
| NG_000006.1:g.37622_37624delinsCGA | |
| NG_059186.1:g.5109_5111delinsCGA |
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.43_45delinsCGA MANE Select | NP_000549.1:p.Trp15Arg |
| ENST00000320868.9:c.43_45delinsCGA MANE Select | ENSP00000322421.5:p.Trp15Arg |
| NM_000558.4:c.43_45delinsCGA | NP_000549.1:p.Trp15Arg |
| ENST00000397797.1:c.-5_-3delinsCGA | ENSP00000380899.1:n.-5_-3delinsCGA |
| ENST00000472694.1:n.62_64delinsCGA | |
| ENST00000487791.1:n.12_14delinsCGA |