Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31271104del , CM000668.2:g.31271104del | GRCh38 |
| NC_000006.11:g.31238881del , CM000668.1:g.31238881del | GRCh37 |
| NC_000006.10:g.31346860del | NCBI36 |
| NG_029422.2:g.6029del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.589del MANE Select | ENSP00000365402.5:p.Glu197ArgfsTer17 | |
| ENST00000376228.9:c.589del | ENSP00000365402.5:p.Glu197ArgfsTer17 | |
| ENST00000376237.8:c.*176del | ENSP00000365412.4:n.*176del | |
| ENST00000383329.7:c.589del | ENSP00000372819.3:p.Glu197ArgfsTer17 | |
| ENST00000415537.1:c.587del | ||
| ENST00000484378.1:n.858del | ||
| ENST00000487245.5:n.948del | ||
| ENST00000495835.1:n.778del | ||
| NM_002117.5:c.589del | NP_002108.4:p.Glu197ArgfsTer17 | |
| NM_002117.6:c.589del MANE Select | NP_002108.4:p.Glu197ArgfsTer17 |