Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25010175_25010176insCCCC , CM000685.2:g.25010175_25010176insCCCC | GRCh38 |
| NC_000023.10:g.25028292_25028293insCCCC , CM000685.1:g.25028292_25028293insCCCC | GRCh37 |
| NC_000023.9:g.24938213_24938214insCCCC | NCBI36 |
| NG_008281.1:g.10774_10775insGGGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.1119+85_1119+86insGGGG MANE Select | ENSP00000368332.4:n.1119+85_1119+86insGGGG | |
| ENST00000379044.4:c.1119+85_1119+86insGGGG | ENSP00000368332.4:n.1119+85_1119+86insGGGG | |
| NM_139058.2:c.1119+85_1119+86insGGGG | NP_620689.1:n.1119+85_1119+86insGGGG | |
| NM_139058.3:c.1119+85_1119+86insGGGG MANE Select | NP_620689.1:n.1119+85_1119+86insGGGG |