Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215817028_215817029delinsCA , CM000663.2:g.215817028_215817029delinsCA | GRCh38 |
| NC_000001.10:g.215990370_215990371delinsCA , CM000663.1:g.215990370_215990371delinsCA | GRCh37 |
| NC_000001.9:g.214056993_214056994delinsCA | NCBI36 |
| NG_009497.1:g.611368_611369delinsTG | |
| NG_009497.2:g.611420_611421delinsTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.9538_9539delinsTG MANE Select | ENSP00000305941.3:p.Cys3180= | |
| ENST00000674083.1:c.9538_9539delinsTG | ENSP00000501296.1:p.Cys3180= | |
| ENST00000307340.7:c.9538_9539delinsTG | ENSP00000305941.3:p.Cys3180= | |
| NM_206933.2:c.9538_9539delinsTG | NP_996816.2:p.Cys3180= | |
| NM_206933.3:c.9538_9539delinsTG | NP_996816.2:p.Cys3180= | |
| NM_206933.4:c.9538_9539delinsTG MANE Select | NP_996816.3:p.Cys3180= |