Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461778del , CM000672.2:g.122461778del | GRCh38 |
| NC_000010.10:g.124221294del , CM000672.1:g.124221294del | GRCh37 |
| NC_000010.9:g.124211284del | NCBI36 |
| NG_011554.1:g.5254del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000368984.8:c.126del MANE Select | ENSP00000357980.3:p.Glu42AspfsTer? | |
| ENST00000648167.1:c.154+3069del | ENSP00000498033.1:n.154+3069del | |
| ENST00000368984.7:c.126del | ENSP00000357980.3:p.Glu42AspfsTer? | |
| NM_002775.4:c.126del | NP_002766.1:p.Glu42AspfsTer? | |
| NM_002775.5:c.126del MANE Select | NP_002766.1:p.Glu42AspfsTer? |