Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584071_41584072insC , CM000679.2:g.41584071_41584072insC | GRCh38 |
| NC_000017.10:g.39740323_39740324insC , CM000679.1:g.39740323_39740324insC | GRCh37 |
| NC_000017.9:g.36993849_36993850insC | NCBI36 |
| NG_008624.1:g.7824_7825insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-151_766-150insG MANE Select | ENSP00000167586.6:n.766-151_766-150insG | |
| ENST00000167586.6:c.766-151_766-150insG | ENSP00000167586.6:n.766-151_766-150insG | |
| ENST00000476662.1:n.216-151_216-150insG | ||
| NM_000526.4:c.766-151_766-150insG | NP_000517.2:n.766-151_766-150insG | |
| NM_000526.5:c.766-151_766-150insG MANE Select | NP_000517.3:n.766-151_766-150insG |