Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40471666dup , CM000677.2:g.40471666dup | GRCh38 |
| NC_000015.9:g.40763865dup , CM000677.1:g.40763865dup | GRCh37 |
| NC_000015.8:g.38551157dup | NCBI36 |
| NG_017074.1:g.5706dup , LRG_600:g.5706dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306243.7:c.453dup MANE Select | ENSP00000307297.6:p.Cys152LeufsTer10 | |
| ENST00000306243.6:c.453dup | ENSP00000307297.5:p.Cys152LeufsTer10 | |
| ENST00000559991.1:c.426+27dup | ENSP00000453882.1:n.426+27dup | |
| NM_130468.3:c.453dup , LRG_600t1:c.453dup | NP_569735.1:p.Cys152LeufsTer10 | |
| NM_130468.4:c.453dup MANE Select | NP_569735.1:p.Cys152LeufsTer10 |