Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133366149del , CM000672.2:g.133366149del | GRCh38 |
| NC_000010.10:g.135179653del , CM000672.1:g.135179653del | GRCh37 |
| NC_000010.9:g.135029643del | NCBI36 |
| NG_042077.1:g.12258del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368547.4:c.620-52del MANE Select | ENSP00000357535.3:n.620-52del | |
| ENST00000368547.3:c.620-52del | ENSP00000357535.3:n.620-52del | |
| NM_004092.3:c.620-52del | NP_004083.3:n.620-52del | |
| XR_002956965.1:n.1424del | ||
| NM_004092.4:c.620-52del MANE Select | NP_004083.3:n.620-52del |