Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781677_94781678insTTAA , CM000672.2:g.94781677_94781678insTTAA | GRCh38 |
| NC_000010.10:g.96541434_96541435insTTAA , CM000672.1:g.96541434_96541435insTTAA | GRCh37 |
| NC_000010.9:g.96531424_96531425insTTAA | NCBI36 |
| NG_008384.2:g.23972_23973insTTAA | |
| NG_008384.3:g.23997_23998insTTAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.643-144_643-143insTTAA MANE Select | ENSP00000360372.3:n.643-144_643-143insTTAA | |
| ENST00000645461.1:n.1696-144_1696-143insTTAA | ||
| ENST00000371321.7:c.643-144_643-143insTTAA | ENSP00000360372.3:n.643-144_643-143insTTAA | |
| ENST00000464755.1:c.1406-144_1406-143insTTAA | ENSP00000483243.1:n.1406-144_1406-143insTTAA | |
| NM_000769.2:c.643-144_643-143insTTAA | NP_000760.1:n.643-144_643-143insTTAA | |
| NM_000769.4:c.643-144_643-143insTTAA MANE Select | NP_000760.1:n.643-144_643-143insTTAA |