Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12717860dup , CM000674.2:g.12717860dup | GRCh38 |
| NC_000012.11:g.12870794dup , CM000674.1:g.12870794dup | GRCh37 |
| NC_000012.10:g.12762061dup | NCBI36 |
| NG_016341.1:g.5493dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.21dup | ENSP00000507272.1:p.Asn8Ter | |
| ENST00000682620.1:n.1631-965dup | ||
| ENST00000684771.1:n.585-965dup | ||
| ENST00000228872.9:c.21dup MANE Select | ENSP00000228872.4:p.Asn8Ter | |
| ENST00000228872.8:c.21dup | ENSP00000228872.4:p.Asn8Ter | |
| ENST00000396340.1:c.21dup | ENSP00000379629.1:p.Asn8Ter | |
| ENST00000477087.1:n.155-965dup | ||
| NM_004064.4:c.21dup | NP_004055.1:p.Asn8Ter | |
| NM_004064.5:c.21dup MANE Select | NP_004055.1:p.Asn8Ter |