Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625424dup , CM000673.2:g.22625424dup | GRCh38 |
| NC_000011.9:g.22646970dup , CM000673.1:g.22646970dup | GRCh37 |
| NC_000011.8:g.22603546dup | NCBI36 |
| NG_007425.1:g.5419dup , LRG_527:g.5419dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.388dup MANE Select | ENSP00000330875.3:p.Gln130ProfsTer23 | |
| ENST00000327470.4:c.388dup | ENSP00000330875.3:p.Gln130ProfsTer23 | |
| NM_022725.3:c.388dup , LRG_527t1:c.388dup | NP_073562.1:p.Gln130ProfsTer23 | |
| NM_022725.4:c.388dup MANE Select | NP_073562.1:p.Gln130ProfsTer23 |