Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.100418059dup , CM000674.2:g.100418059dup | GRCh38 |
| NC_000012.11:g.100811837dup , CM000674.1:g.100811837dup | GRCh37 |
| NC_000012.10:g.99335968dup | NCBI36 |
| NG_021175.1:g.65981dup |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_139319.3:c.1328dup MANE Select | NP_647480.1:p.Arg444ThrfsTer? |
| ENST00000323346.10:c.1328dup MANE Select | ENSP00000316909.4:p.Arg444ThrfsTer? |
| NM_001145288.1:c.1178dup | NP_001138760.1:p.Arg394ThrfsTer? |
| NM_001145288.2:c.1178dup | NP_001138760.1:p.Arg394ThrfsTer? |
| NM_139319.2:c.1328dup | NP_647480.1:p.Arg444ThrfsTer? |
| ENST00000323346.9:c.1328dup | ENSP00000316909.4:p.Arg444ThrfsTer? |
| ENST00000392989.3:c.1178dup | ENSP00000376715.3:p.Arg394ThrfsTer? |
| ENST00000552697.1:n.221dup |