| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24290788del , CM000668.2:g.24290788del | GRCh38 |
| NC_000006.11:g.24291016del , CM000668.1:g.24291016del | GRCh37 |
| NC_000006.10:g.24398995del | NCBI36 |
| NG_012829.1:g.72265del | |
| NG_012829.2:g.97505del |
| HGVS | Amino-acid Change |
|---|---|
| NM_016356.5:c.704+144del MANE Select | NP_057440.2:n.704+144del |
| ENST00000378454.8:c.704+144del MANE Select | ENSP00000367715.3:n.704+144del |
| NM_001195610.1:c.704+144del | NP_001182539.1:n.704+144del |
| NM_001195610.2:c.704+144del | NP_001182539.1:n.704+144del |
| NM_016356.4:c.704+144del | NP_057440.2:n.704+144del |
| ENST00000378454.7:c.704+144del | ENSP00000367715.3:n.704+144del |