Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74751960_74751961insTTGC , CM000677.2:g.74751960_74751961insTTGC | GRCh38 |
| NC_000015.9:g.75044301_75044302insTTGC , CM000677.1:g.75044301_75044302insTTGC | GRCh37 |
| NC_000015.8:g.72831354_72831355insTTGC | NCBI36 |
| NG_008431.1:g.34419_34420insTTGC | |
| NG_008431.2:g.34419_34420insTTGC | |
| NG_061543.1:g.8116_8117insTTGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.1042+106_1042+107insTTGC MANE Select | ENSP00000342007.4:n.1042+106_1042+107insTTGC | |
| ENST00000343932.4:c.1042+106_1042+107insTTGC | ENSP00000342007.4:n.1042+106_1042+107insTTGC | |
| NM_000761.4:c.1042+106_1042+107insTTGC | NP_000752.2:n.1042+106_1042+107insTTGC | |
| NM_000761.5:c.1042+106_1042+107insTTGC MANE Select | NP_000752.2:n.1042+106_1042+107insTTGC |