Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.75210895_75210896insGG , CM000680.2:g.75210895_75210896insGG | GRCh38 |
| NC_000018.9:g.72922850_72922851insGG , CM000680.1:g.72922850_72922851insGG | GRCh37 |
| NC_000018.8:g.71051838_71051839insGG | NCBI36 |
| NG_032047.1:g.5141_5142insGG |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001308210.2:c.-982_-981insGG MANE Select | NP_001295139.1:n.-982_-981insGG |
| ENST00000580243.3:c.-982_-981insGG MANE Select | ENSP00000464391.1:n.-982_-981insGG |
| NM_005786.5:c.-444_-443insGG | NP_005777.3:n.-444_-443insGG |
| NM_005786.6:c.-444_-443insGG | NP_005777.3:n.-444_-443insGG |
| ENST00000322038.5:c.-444_-443insGG | ENSP00000323584.5:n.-444_-443insGG |