Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124875593dup , CM000673.2:g.124875593dup | GRCh38 |
| NC_000011.9:g.124745489dup , CM000673.1:g.124745489dup | GRCh37 |
| NC_000011.8:g.124250699dup | NCBI36 |
| NG_016214.1:g.15185dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.2329dup MANE Select | ENSP00000380903.1:p.Val777GlyfsTer6 | |
| ENST00000397801.5:c.2329dup | ENSP00000380903.1:p.Val777GlyfsTer6 | |
| ENST00000538940.5:c.2263dup | ENSP00000441797.1:p.Val755GlyfsTer6 | |
| NM_022370.3:c.2329dup | NP_071765.2:p.Val777GlyfsTer6 | |
| XM_011542953.1:c.3301dup | XP_011541255.1:p.Val1101GlyfsTer6 | |
| XM_017018122.1:c.2263dup | XP_016873611.1:p.Val755GlyfsTer6 | |
| NM_022370.4:c.2329dup MANE Select | NP_071765.2:p.Val777GlyfsTer6 |