Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.46411835del , CM000681.2:g.46411835del | GRCh38 |
| NC_000019.9:g.46915092del , CM000681.1:g.46915092del | GRCh37 |
| NC_000019.8:g.51606932del | NCBI36 |
| NG_031956.1:g.6828del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032040.5:c.976del MANE Select | NP_114429.2:p.Asp326ThrfsTer? |
| ENST00000307522.5:c.976del MANE Select | ENSP00000303158.3:p.Asp326ThrfsTer? |
| NM_032040.4:c.976del | NP_114429.2:p.Asp326ThrfsTer? |
| ENST00000307522.3:c.976del | ENSP00000303158.3:p.Asp326ThrfsTer? |
| ENST00000697726.1:c.1186del | ENSP00000513420.1:p.Asp396ThrfsTer? |