Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154188000dup , CM000685.2:g.154188000dup | GRCh38 |
| NC_000023.10:g.153453489dup , CM000685.1:g.153453489dup | GRCh37 |
| NG_011606.1:g.10405dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000595290.6:c.343dup MANE Select | ENSP00000472316.1:p.Val115GlyfsTer? | |
| ENST00000595290.5:c.343dup | ENSP00000472316.1:p.Val115GlyfsTer? | |
| ENST00000595330.1:n.353dup | ||
| NM_000513.2:c.343dup MANE Select | NP_000504.1:p.Val115GlyfsTer? |