Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583310_41583314del , CM000679.2:g.41583310_41583314del | GRCh38 |
| NC_000017.10:g.39739562_39739566del , CM000679.1:g.39739562_39739566del | GRCh37 |
| NC_000017.9:g.36993088_36993092del | NCBI36 |
| NG_008624.1:g.8582_8586del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.1195_1199del MANE Select | ENSP00000167586.6:p.Lys399ProfsTer? | |
| ENST00000167586.6:c.1195_1199del | ENSP00000167586.6:p.Lys399ProfsTer? | |
| ENST00000441550.2:n.142_146del | ||
| ENST00000476662.1:n.645_649del | ||
| NM_000526.4:c.1195_1199del | NP_000517.2:p.Lys399ProfsTer? | |
| NM_000526.5:c.1195_1199del MANE Select | NP_000517.3:p.Lys399ProfsTer? |