Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536258del , CM000679.2:g.42536258del | GRCh38 |
| NC_000017.10:g.40688276del , CM000679.1:g.40688276del | GRCh37 |
| NC_000017.9:g.37941802del | NCBI36 |
| NG_011552.1:g.5326del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.-15del MANE Select | ENSP00000225927.1:n.-15del | |
| ENST00000225927.6:c.-15del | ENSP00000225927.1:n.-15del | |
| NM_000263.3:c.-15del | NP_000254.2:n.-15del | |
| XM_024450771.1:c.-15del | XP_024306539.1:n.-15del | |
| NM_000263.4:c.-15del MANE Select | NP_000254.2:n.-15del |