Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78118182_78118183insA , CM000685.2:g.78118182_78118183insA | GRCh38 |
| NC_000023.10:g.77373679_77373680insA , CM000685.1:g.77373679_77373680insA | GRCh37 |
| NC_000023.9:g.77260335_77260336insA | NCBI36 |
| NG_008862.1:g.19014_19015insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.641+12_641+13insA MANE Select | ENSP00000362413.4:n.641+12_641+13insA | |
| ENST00000644362.1:c.557+12_557+13insA | ENSP00000496140.1:n.557+12_557+13insA | |
| ENST00000373316.4:c.641+12_641+13insA | ENSP00000362413.4:n.641+12_641+13insA | |
| ENST00000491291.1:n.633+12_633+13insA | ||
| NM_000291.3:c.641+12_641+13insA | NP_000282.1:n.641+12_641+13insA | |
| NM_000291.4:c.641+12_641+13insA MANE Select | NP_000282.1:n.641+12_641+13insA |