Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584058_41584059insGT , CM000679.2:g.41584058_41584059insGT | GRCh38 |
| NC_000017.10:g.39740310_39740311insGT , CM000679.1:g.39740310_39740311insGT | GRCh37 |
| NC_000017.9:g.36993836_36993837insGT | NCBI36 |
| NG_008624.1:g.7838_7839insCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-137_766-136insCA MANE Select | ENSP00000167586.6:n.766-137_766-136insCA | |
| ENST00000167586.6:c.766-137_766-136insCA | ENSP00000167586.6:n.766-137_766-136insCA | |
| ENST00000476662.1:n.216-137_216-136insCA | ||
| NM_000526.4:c.766-137_766-136insCA | NP_000517.2:n.766-137_766-136insCA | |
| NM_000526.5:c.766-137_766-136insCA MANE Select | NP_000517.3:n.766-137_766-136insCA |