Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583977_41583978delinsGT , CM000679.2:g.41583977_41583978delinsGT | GRCh38 |
| NC_000017.10:g.39740229_39740230delinsGT , CM000679.1:g.39740229_39740230delinsGT | GRCh37 |
| NC_000017.9:g.36993755_36993756delinsGT | NCBI36 |
| NG_008624.1:g.7918_7919delinsAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-57_766-56delinsAC MANE Select | ENSP00000167586.6:n.766-57_766-56delinsAC | |
| ENST00000167586.6:c.766-57_766-56delinsAC | ENSP00000167586.6:n.766-57_766-56delinsAC | |
| ENST00000476662.1:n.216-57_216-56delinsAC | ||
| NM_000526.4:c.766-57_766-56delinsAC | NP_000517.2:n.766-57_766-56delinsAC | |
| NM_000526.5:c.766-57_766-56delinsAC MANE Select | NP_000517.3:n.766-57_766-56delinsAC |