Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68647133dup , CM000666.2:g.68647133dup | GRCh38 |
| NC_000004.11:g.69512851dup , CM000666.1:g.69512851dup | GRCh37 |
| NC_000004.10:g.69195446dup | NCBI36 |
| NG_052676.1:g.28649dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.1569dup MANE Select | ENSP00000341045.5:p.Gly524ArgfsTer14 | |
| ENST00000338206.5:c.1569dup | ENSP00000341045.5:p.Gly524ArgfsTer14 | |
| ENST00000616841.4:c.1569dup | ENSP00000482004.1:p.Gly524ArgfsTer14 | |
| NM_001076.3:c.1569dup | NP_001067.2:p.Gly524ArgfsTer14 | |
| NM_001076.4:c.1569dup MANE Select | NP_001067.2:p.Gly524ArgfsTer14 |