Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583264_41583273del , CM000679.2:g.41583264_41583273del | GRCh38 |
| NC_000017.10:g.39739516_39739525del , CM000679.1:g.39739516_39739525del | GRCh37 |
| NC_000017.9:g.36993042_36993051del | NCBI36 |
| NG_008624.1:g.8627_8636del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000167586.7:c.1240_1249del MANE Select | ENSP00000167586.6:p.Thr414AlafsTer25 | |
| ENST00000167586.6:c.1240_1249del | ENSP00000167586.6:p.Thr414AlafsTer25 | |
| ENST00000441550.2:n.187_196del | ||
| ENST00000476662.1:n.690_699del | ||
| NM_000526.4:c.1240_1249del | NP_000517.2:p.Thr414AlafsTer25 | |
| NM_000526.5:c.1240_1249del MANE Select | NP_000517.3:p.Thr414AlafsTer25 |