Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6022071_6022072delinsTC , CM000674.2:g.6022071_6022072delinsTC | GRCh38 |
| NC_000012.11:g.6131237_6131238delinsTC , CM000674.1:g.6131237_6131238delinsTC | GRCh37 |
| NC_000012.10:g.6001498_6001499delinsTC | NCBI36 |
| NG_009072.1:g.107599_107600delinsGA | |
| NG_009072.2:g.107599_107600delinsGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.3539-37_3539-36delinsGA MANE Select | ENSP00000261405.5:n.3539-37_3539-36delinsGA | |
| ENST00000261405.9:c.3539-37_3539-36delinsGA | ENSP00000261405.5:n.3539-37_3539-36delinsGA | |
| ENST00000538635.5:n.421-28138_421-28137delinsGA | ||
| NM_000552.3:c.3539-37_3539-36delinsGA | NP_000543.2:n.3539-37_3539-36delinsGA | |
| NM_000552.4:c.3539-37_3539-36delinsGA | NP_000543.2:n.3539-37_3539-36delinsGA | |
| NM_000552.5:c.3539-37_3539-36delinsGA MANE Select | NP_000543.3:n.3539-37_3539-36delinsGA |