Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755100_74755102del , CM000677.2:g.74755100_74755102del | GRCh38 |
| NC_000015.9:g.75047441_75047443del , CM000677.1:g.75047441_75047443del | GRCh37 |
| NC_000015.8:g.72834494_72834496del | NCBI36 |
| NG_008431.1:g.37559_37561del | |
| NG_008431.2:g.37559_37561del | |
| NG_061543.1:g.11256_11258del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.*12_*14del MANE Select | ENSP00000342007.4:n.*12_*14del | |
| ENST00000343932.4:c.*12_*14del | ENSP00000342007.4:n.*12_*14del | |
| NM_000761.4:c.*12_*14del | NP_000752.2:n.*12_*14del | |
| NM_000761.5:c.*12_*14del MANE Select | NP_000752.2:n.*12_*14del |