Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584082_41584083insC , CM000679.2:g.41584082_41584083insC | GRCh38 |
| NC_000017.10:g.39740334_39740335insC , CM000679.1:g.39740334_39740335insC | GRCh37 |
| NC_000017.9:g.36993860_36993861insC | NCBI36 |
| NG_008624.1:g.7813_7814insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-162_766-161insG MANE Select | ENSP00000167586.6:n.766-162_766-161insG | |
| ENST00000167586.6:c.766-162_766-161insG | ENSP00000167586.6:n.766-162_766-161insG | |
| ENST00000476662.1:n.216-162_216-161insG | ||
| NM_000526.4:c.766-162_766-161insG | NP_000517.2:n.766-162_766-161insG | |
| NM_000526.5:c.766-162_766-161insG MANE Select | NP_000517.3:n.766-162_766-161insG |