Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215867205_215867206insAGG , CM000663.2:g.215867205_215867206insAGG | GRCh38 |
| NC_000001.10:g.216040547_216040548insAGG , CM000663.1:g.216040547_216040548insAGG | GRCh37 |
| NC_000001.9:g.214107170_214107171insAGG | NCBI36 |
| NG_009497.1:g.561191_561192insCCT | |
| NG_009497.2:g.561243_561244insCCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.8682-36_8682-35insCCT MANE Select | ENSP00000305941.3:n.8682-36_8682-35insCCT | |
| ENST00000674083.1:c.8682-36_8682-35insCCT | ENSP00000501296.1:n.8682-36_8682-35insCCT | |
| ENST00000307340.7:c.8682-36_8682-35insCCT | ENSP00000305941.3:n.8682-36_8682-35insCCT | |
| NM_206933.2:c.8682-36_8682-35insCCT | NP_996816.2:n.8682-36_8682-35insCCT | |
| NM_206933.3:c.8682-36_8682-35insCCT | NP_996816.2:n.8682-36_8682-35insCCT | |
| NM_206933.4:c.8682-36_8682-35insCCT MANE Select | NP_996816.3:n.8682-36_8682-35insCCT |