Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128852918T= , CM000669.2:g.128852918T= | GRCh38 |
| NC_000007.13:g.128492972T= , CM000669.1:g.128492972T= | GRCh37 |
| NC_000007.12:g.128280208T= | NCBI36 |
| NG_011807.1:g.27490T= , LRG_870:g.27490T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.6095T= (FLNC) MANE Select | ENSP00000327145.8:p.Leu2032= | |
| ENST00000325888.12:c.6095T= (FLNC) | ENSP00000327145.8:p.Leu2032= | |
| ENST00000346177.6:c.5996T= (FLNC) | ENSP00000344002.6:p.Leu1999= | |
| NM_001127487.1:c.5996T= (FLNC) | NP_001120959.1:p.Leu1999= | |
| NM_001458.4:c.6095T= , LRG_870t1:c.6095T= (FLNC) | NP_001449.3:p.Leu2032= | |
| NR_149055.1:n.215+367A= (FLNC-AS1) | ||
| NM_001127487.2:c.5996T= (FLNC) | NP_001120959.1:p.Leu1999= | |
| NM_001458.5:c.6095T= (FLNC) MANE Select | NP_001449.3:p.Leu2032= |