Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270032dup , CM000668.2:g.31270032dup | GRCh38 |
| NC_000006.11:g.31237809dup , CM000668.1:g.31237809dup | GRCh37 |
| NC_000006.10:g.31345788dup | NCBI36 |
| NG_029422.2:g.7100dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.949dup MANE Select | ENSP00000365402.5:p.Val317GlyfsTer18 | |
| ENST00000376228.9:c.949dup | ENSP00000365402.5:p.Val317GlyfsTer18 | |
| ENST00000376237.8:c.*536dup | ENSP00000365412.4:n.*536dup | |
| ENST00000383329.7:c.949dup | ENSP00000372819.3:p.Val317GlyfsTer18 | |
| ENST00000470363.5:n.267dup | ||
| ENST00000487245.5:n.1308dup | ||
| NM_002117.5:c.949dup | NP_002108.4:p.Val317GlyfsTer18 | |
| NM_002117.6:c.949dup MANE Select | NP_002108.4:p.Val317GlyfsTer18 |