Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584054_41584055insG , CM000679.2:g.41584054_41584055insG | GRCh38 |
| NC_000017.10:g.39740306_39740307insG , CM000679.1:g.39740306_39740307insG | GRCh37 |
| NC_000017.9:g.36993832_36993833insG | NCBI36 |
| NG_008624.1:g.7841_7842insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-134_766-133insC MANE Select | ENSP00000167586.6:n.766-134_766-133insC | |
| ENST00000167586.6:c.766-134_766-133insC | ENSP00000167586.6:n.766-134_766-133insC | |
| ENST00000476662.1:n.216-134_216-133insC | ||
| NM_000526.4:c.766-134_766-133insC | NP_000517.2:n.766-134_766-133insC | |
| NM_000526.5:c.766-134_766-133insC MANE Select | NP_000517.3:n.766-134_766-133insC |