Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73323790dup , CM000677.2:g.73323790dup | GRCh38 |
| NC_000015.9:g.73616131dup , CM000677.1:g.73616131dup | GRCh37 |
| NC_000015.8:g.71403184dup | NCBI36 |
| NG_009063.1:g.50479dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.2307dup MANE Select | ENSP00000261917.3:p.Thr770HisfsTer? | |
| ENST00000261917.3:c.2307dup | ENSP00000261917.3:p.Thr770HisfsTer? | |
| NM_005477.2:c.2307dup | NP_005468.1:p.Thr770HisfsTer? | |
| XM_011521148.1:c.1089dup | XP_011519450.1:p.Thr364HisfsTer? | |
| XM_011521148.2:c.1089dup | XP_011519450.1:p.Thr364HisfsTer? | |
| NM_005477.3:c.2307dup MANE Select | NP_005468.1:p.Thr770HisfsTer? |