Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.43068078del , CM000677.2:g.43068078del | GRCh38 |
| NC_000015.9:g.43360276del , CM000677.1:g.43360276del | GRCh37 |
| NC_000015.8:g.41147568del | NCBI36 |
| NG_012182.1:g.43011del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290650.9:c.660-42del MANE Select | ENSP00000290650.4:n.660-42del | |
| ENST00000290650.8:c.660-42del | ENSP00000290650.4:n.660-42del | |
| ENST00000546274.6:c.660-42del | ENSP00000477932.1:n.660-42del | |
| ENST00000563239.1:c.*202+2821del | ENSP00000456502.1:n.*202+2821del | |
| NM_174916.2:c.660-42del | NP_777576.1:n.660-42del | |
| NM_174916.3:c.660-42del MANE Select | NP_777576.1:n.660-42del |