Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990539_45990540insCT , CM000683.2:g.45990539_45990540insCT | GRCh38 |
| NC_000021.8:g.47410453_47410454insCT , CM000683.1:g.47410453_47410454insCT | GRCh37 |
| NC_000021.7:g.46234881_46234882insCT | NCBI36 |
| NG_008674.1:g.13791_13792insCT , LRG_475:g.13791_13792insCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1002+117_1002+118insCT MANE Select | ENSP00000355180.3:n.1002+117_1002+118insCT | |
| ENST00000361866.7:c.1002+117_1002+118insCT | ENSP00000355180.3:n.1002+117_1002+118insCT | |
| ENST00000612273.1:c.1002+117_1002+118insCT | ENSP00000483630.1:n.1002+117_1002+118insCT | |
| NM_001848.2:c.1002+117_1002+118insCT , LRG_475t1:c.1002+117_1002+118insCT | NP_001839.2:n.1002+117_1002+118insCT | |
| NM_001848.3:c.1002+117_1002+118insCT MANE Select | NP_001839.2:n.1002+117_1002+118insCT |