Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172968del , CM000678.2:g.172968del | GRCh38 |
| NC_000016.9:g.222967del , CM000678.1:g.222967del | GRCh37 |
| NC_000016.8:g.162967del | NCBI36 |
| NG_000006.1:g.33831del | |
| NG_059186.1:g.1318del | |
| NG_059271.1:g.5122del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.56del MANE Select | NP_000508.1:p.Gly19AlafsTer? |
| ENST00000251595.11:c.56del MANE Select | ENSP00000251595.6:p.Gly19AlafsTer? |
| NM_000517.4:c.56del | NP_000508.1:p.Gly19AlafsTer? |
| ENST00000251595.10:c.56del | ENSP00000251595.6:p.Gly19AlafsTer? |
| ENST00000397806.1:c.-2+10del | ENSP00000380908.1:n.-2+10del |
| ENST00000482565.1:n.75del | |
| ENST00000484216.1:n.25del |