Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46853665_46853666insA , CM000685.2:g.46853665_46853666insA | GRCh38 |
| NC_000023.10:g.46713100_46713101insA , CM000685.1:g.46713100_46713101insA | GRCh37 |
| NC_000023.9:g.46598044_46598045insA | NCBI36 |
| NG_009107.1:g.21754_21755insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218340.4:c.292_293insA MANE Select | ENSP00000218340.3:p.Gly98GlufsTer26 | |
| ENST00000218340.3:c.292_293insA | ENSP00000218340.3:p.Gly98GlufsTer26 | |
| NM_006915.2:c.292_293insA | NP_008846.2:p.Gly98GlufsTer26 | |
| NM_006915.3:c.292_293insA MANE Select | NP_008846.2:p.Gly98GlufsTer26 |