Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.82148514_82148515delinsCA , CM000678.2:g.82148514_82148515delinsCA | GRCh38 |
| NC_000016.9:g.82182119_82182120delinsCA , CM000678.1:g.82182119_82182120delinsCA | GRCh37 |
| NC_000016.8:g.80739620_80739621delinsCA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258169.9:c.*216_*217delinsTG MANE Select | ENSP00000258169.4:n.*216_*217delinsTG | |
| ENST00000258169.8:c.*216_*217delinsTG | ENSP00000258169.4:n.*216_*217delinsTG | |
| ENST00000563100.5:c.*72+144_*72+145delinsTG | ENSP00000454996.1:n.*72+144_*72+145delinsTG | |
| NM_005792.2:c.*216_*217delinsTG MANE Select | NP_005783.2:n.*216_*217delinsTG | |
| XM_011522808.1:c.*216_*217delinsTG | XP_011521110.1:n.*216_*217delinsTG | |
| XM_011522808.3:c.*216_*217delinsTG | XP_011521110.1:n.*216_*217delinsTG |