Linked Data
gnomAD v4:
7-128858544-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128858544G>A , CM000669.2:g.128858544G>A | GRCh38 |
| NC_000007.13:g.128498598G>A , CM000669.1:g.128498598G>A | GRCh37 |
| NC_000007.12:g.128285834G>A | NCBI36 |
| NG_011807.1:g.33116G>A , LRG_870:g.33116G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.*21G>A (FLNC) MANE Select | ENSP00000327145.8:n.*21G>A | |
| ENST00000325888.12:c.*21G>A (FLNC) | ENSP00000327145.8:n.*21G>A | |
| ENST00000346177.6:c.*21G>A (FLNC) | ENSP00000344002.6:n.*21G>A | |
| NM_001127487.1:c.*21G>A (FLNC) | NP_001120959.1:n.*21G>A | |
| NM_001458.4:c.*21G>A , LRG_870t1:c.*21G>A (FLNC) | NP_001449.3:n.*21G>A | |
| NR_149055.1:n.102+3981C>T (FLNC-AS1) | ||
| NM_001127487.2:c.*21G>A (FLNC) | NP_001120959.1:n.*21G>A | |
| NM_001458.5:c.*21G>A (FLNC) MANE Select | NP_001449.3:n.*21G>A |