Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128858466T= , CM000669.2:g.128858466T= | GRCh38 |
| NC_000007.13:g.128498520T= , CM000669.1:g.128498520T= | GRCh37 |
| NC_000007.12:g.128285756T= | NCBI36 |
| NG_011807.1:g.33038T= , LRG_870:g.33038T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.8121T= (FLNC) MANE Select | ENSP00000327145.8:p.Ile2707= | |
| ENST00000325888.12:c.8121T= (FLNC) | ENSP00000327145.8:p.Ile2707= | |
| ENST00000346177.6:c.8022T= (FLNC) | ENSP00000344002.6:p.Ile2674= | |
| NM_001127487.1:c.8022T= (FLNC) | NP_001120959.1:p.Ile2674= | |
| NM_001458.4:c.8121T= , LRG_870t1:c.8121T= (FLNC) | NP_001449.3:p.Ile2707= | |
| NR_149055.1:n.102+4059A= (FLNC-AS1) | ||
| NM_001127487.2:c.8022T= (FLNC) | NP_001120959.1:p.Ile2674= | |
| NM_001458.5:c.8121T= (FLNC) MANE Select | NP_001449.3:p.Ile2707= |