Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431805dup , CM000663.2:g.229431805dup | GRCh38 |
| NC_000001.10:g.229567552dup , CM000663.1:g.229567552dup | GRCh37 |
| NC_000001.9:g.227634175dup | NCBI36 |
| NG_006672.1:g.7297dup , LRG_429:g.7297dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.911dup | ENSP00000355644.4:p.Thr305HisfsTer9 | |
| ENST00000684723.1:c.776dup | ENSP00000508084.1:p.Thr260HisfsTer9 | |
| ENST00000366683.3:c.542dup | ENSP00000355644.3:p.Thr182HisfsTer9 | |
| ENST00000366684.7:c.911dup MANE Select | ENSP00000355645.3:p.Thr305HisfsTer9 | |
| NM_001100.3:c.911dup , LRG_429t1:c.911dup | NP_001091.1:p.Thr305HisfsTer9 | |
| NM_001100.4:c.911dup MANE Select | NP_001091.1:p.Thr305HisfsTer9 |