Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128852591dup , CM000669.2:g.128852591dup | GRCh38 |
| NC_000007.13:g.128492645dup , CM000669.1:g.128492645dup | GRCh37 |
| NC_000007.12:g.128279881dup | NCBI36 |
| NG_011807.1:g.27163dup , LRG_870:g.27163dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.5843dup (FLNC) | ||
| ENST00000325888.12:c.5843dup (FLNC) | ||
| ENST00000346177.6:c.5744dup (FLNC) | ||
| NM_001127487.1:c.5744dup (FLNC) | ||
| NM_001458.4:c.5843dup , LRG_870t1:c.5843dup (FLNC) | ||
| NR_149055.1:n.215+695dup (FLNC-AS1) | ||
| NM_001127487.2:c.5744dup (FLNC) | ||
| NM_001458.5:c.5843dup (FLNC) |