Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.45462026_45462027insTG , CM000667.2:g.45462026_45462027insTG | GRCh38 |
| NC_000005.9:g.45462128_45462129insTG , CM000667.1:g.45462128_45462129insTG | GRCh37 |
| NC_000005.8:g.45497885_45497886insTG | NCBI36 |
| NG_042183.1:g.239092_239093insCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303230.6:c.850-20_850-19insCA MANE Select | ENSP00000307342.4:n.850-20_850-19insCA | |
| ENST00000637305.1:n.13-20_13-19insCA | ||
| ENST00000673735.1:c.850-20_850-19insCA | ENSP00000501107.1:n.850-20_850-19insCA | |
| ENST00000303230.5:c.850-20_850-19insCA | ENSP00000307342.4:n.850-20_850-19insCA | |
| NM_021072.3:c.850-20_850-19insCA | NP_066550.2:n.850-20_850-19insCA | |
| NM_021072.4:c.850-20_850-19insCA MANE Select | NP_066550.2:n.850-20_850-19insCA |