Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520164del , CM000674.2:g.52520164del | GRCh38 |
| NC_000012.11:g.52913948del , CM000674.1:g.52913948del | GRCh37 |
| NC_000012.10:g.51200215del | NCBI36 |
| NG_008297.1:g.5297del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000424.4:c.134del MANE Select | NP_000415.2:p.Gly45AlafsTer? |
| ENST00000252242.9:c.134del MANE Select | ENSP00000252242.4:p.Gly45AlafsTer? |
| NM_000424.3:c.134del | NP_000415.2:p.Gly45AlafsTer? |
| ENST00000252242.8:c.134del | ENSP00000252242.4:p.Gly45AlafsTer? |
| ENST00000546577.1:c.134del | ENSP00000449651.1:p.Gly45AlafsTer? |
| ENST00000549420.1:c.43+91del | ENSP00000447209.1:n.43+91del |
| ENST00000551275.1:c.134del | ENSP00000448041.1:p.Gly45AlafsTer? |
| ENST00000552629.5:n.232del |