Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586743del , CM000679.2:g.41586743del | GRCh38 |
| NC_000017.10:g.39742995del , CM000679.1:g.39742995del | GRCh37 |
| NC_000017.9:g.36996521del | NCBI36 |
| NG_008624.1:g.5153del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000526.5:c.92del MANE Select | NP_000517.3:p.Ile31ThrfsTer? |
| ENST00000167586.7:c.92del MANE Select | ENSP00000167586.6:p.Ile31ThrfsTer? |
| NM_000526.4:c.92del | NP_000517.2:p.Ile31ThrfsTer? |
| ENST00000167586.6:c.92del | ENSP00000167586.6:p.Ile31ThrfsTer? |