Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429970_68429971insACT , CM000663.2:g.68429970_68429971insACT | GRCh38 |
| NC_000001.10:g.68895653_68895654insACT , CM000663.1:g.68895653_68895654insACT | GRCh37 |
| NC_000001.9:g.68668241_68668242insACT | NCBI36 |
| NG_008472.1:g.24989_24990insAGT | |
| NG_008472.2:g.24989_24990insAGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1451-44_1451-43insAGT MANE Select | ENSP00000262340.5:n.1451-44_1451-43insAGT | |
| ENST00000262340.5:c.1451-44_1451-43insAGT | ENSP00000262340.5:n.1451-44_1451-43insAGT | |
| NM_000329.2:c.1451-44_1451-43insAGT | NP_000320.1:n.1451-44_1451-43insAGT | |
| XM_017002027.1:c.1175-44_1175-43insAGT | XP_016857516.1:n.1175-44_1175-43insAGT | |
| NM_000329.3:c.1451-44_1451-43insAGT MANE Select | NP_000320.1:n.1451-44_1451-43insAGT |