Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71030586del , CM000666.2:g.71030586del | GRCh38 |
| NC_000004.11:g.71896303del , CM000666.1:g.71896303del | GRCh37 |
| NC_000004.10:g.72115167del | NCBI36 |
| NG_023303.1:g.42039del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000286648.10:c.*1208del MANE Select | ENSP00000286648.5:n.*1208del | |
| ENST00000286648.9:c.*1208del | ENSP00000286648.5:n.*1208del | |
| ENST00000503359.5:c.*1935del | ENSP00000426389.1:n.*1935del | |
| ENST00000504730.5:c.*1275del | ENSP00000425578.1:n.*1275del | |
| ENST00000504952.1:c.*1134del | ENSP00000421508.1:n.*1134del | |
| NM_000788.2:c.*1208del | NP_000779.1:n.*1208del | |
| NM_000788.3:c.*1208del MANE Select | NP_000779.1:n.*1208del |