Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814064del , CM000664.2:g.218814064del | GRCh38 |
| NC_000002.11:g.219678787del , CM000664.1:g.219678787del | GRCh37 |
| NC_000002.10:g.219387031del | NCBI36 |
| NG_007959.1:g.37316del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1061del MANE Select | ENSP00000258415.4:p.Asp354AlafsTer? | |
| ENST00000258415.8:c.1061del | ENSP00000258415.4:p.Asp354AlafsTer? | |
| ENST00000445971.1:c.*522del | ENSP00000404945.1:n.*522del | |
| ENST00000466602.1:n.1183del | ||
| ENST00000494263.5:n.1495del | ||
| NM_000784.3:c.1061del | NP_000775.1:p.Asp354AlafsTer? | |
| XM_017003488.2:c.641del | XP_016858977.1:p.Asp214AlafsTer? | |
| NM_000784.4:c.1061del MANE Select | NP_000775.1:p.Asp354AlafsTer? |