Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584046_41584049del , CM000679.2:g.41584046_41584049del | GRCh38 |
| NC_000017.10:g.39740298_39740301del , CM000679.1:g.39740298_39740301del | GRCh37 |
| NC_000017.9:g.36993824_36993827del | NCBI36 |
| NG_008624.1:g.7859_7862del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-116_766-113del MANE Select | ENSP00000167586.6:n.766-116_766-113del | |
| ENST00000167586.6:c.766-116_766-113del | ENSP00000167586.6:n.766-116_766-113del | |
| ENST00000476662.1:n.216-116_216-113del | ||
| NM_000526.4:c.766-116_766-113del | NP_000517.2:n.766-116_766-113del | |
| NM_000526.5:c.766-116_766-113del MANE Select | NP_000517.3:n.766-116_766-113del |