Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814180_218814182delinsACT , CM000664.2:g.218814180_218814182delinsACT | GRCh38 |
| NC_000002.11:g.219678903_219678905delinsACT , CM000664.1:g.219678903_219678905delinsACT | GRCh37 |
| NC_000002.10:g.219387147_219387149delinsACT | NCBI36 |
| NG_007959.1:g.37432_37434delinsACT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1177_1179delinsACT MANE Select | ENSP00000258415.4:p.Thr393= | |
| ENST00000258415.8:c.1177_1179delinsACT | ENSP00000258415.4:p.Thr393= | |
| ENST00000494263.5:n.1611_1613delinsACT | ||
| NM_000784.3:c.1177_1179delinsACT | NP_000775.1:p.Thr393= | |
| XM_017003488.2:c.757_759delinsACT | XP_016858977.1:p.Thr253= | |
| NM_000784.4:c.1177_1179delinsACT MANE Select | NP_000775.1:p.Thr393= |