Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658987_10658988insG , CM000682.2:g.10658987_10658988insG | GRCh38 |
| NC_000020.10:g.10639635_10639636insG , CM000682.1:g.10639635_10639636insG | GRCh37 |
| NC_000020.9:g.10587635_10587636insG | NCBI36 |
| NG_007496.1:g.20059_20060insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.440-266_440-265insC MANE Select | ENSP00000254958.4:n.440-266_440-265insC | |
| ENST00000254958.9:c.440-266_440-265insC | ENSP00000254958.4:n.440-266_440-265insC | |
| ENST00000423891.6:n.306-266_306-265insC | ||
| NM_000214.2:c.440-266_440-265insC | NP_000205.1:n.440-266_440-265insC | |
| NM_000214.3:c.440-266_440-265insC MANE Select | NP_000205.1:n.440-266_440-265insC |