Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.27095694_27095695insTGT , CM000669.2:g.27095694_27095695insTGT | GRCh38 |
| NC_000007.13:g.27135313_27135314insTGT , CM000669.1:g.27135313_27135314insTGT | GRCh37 |
| NC_000007.12:g.27101838_27101839insTGT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643460.2:c.218_219insACA MANE Select | ENSP00000494260.2:p.Arg73_His74insHis | |
| ENST00000343060.4:c.218_219insACA | ENSP00000343246.4:p.Arg73_His74insHis | |
| ENST00000355633.5:c.218_219insACA | ENSP00000347851.5:p.Arg73_His74insHis | |
| NM_005522.5:c.218_219insACA MANE Select | NP_005513.2:p.Arg73_His74insHis | |
| NM_153620.3:c.218_219insACA | NP_705873.3:p.Arg73_His74insHis |