Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584092_41584093insC , CM000679.2:g.41584092_41584093insC | GRCh38 |
| NC_000017.10:g.39740344_39740345insC , CM000679.1:g.39740344_39740345insC | GRCh37 |
| NC_000017.9:g.36993870_36993871insC | NCBI36 |
| NG_008624.1:g.7803_7804insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.765+164_765+165insG MANE Select | ENSP00000167586.6:n.765+164_765+165insG | |
| ENST00000167586.6:c.765+164_765+165insG | ENSP00000167586.6:n.765+164_765+165insG | |
| ENST00000476662.1:n.215+164_215+165insG | ||
| NM_000526.4:c.765+164_765+165insG | NP_000517.2:n.765+164_765+165insG | |
| NM_000526.5:c.765+164_765+165insG MANE Select | NP_000517.3:n.765+164_765+165insG |