Linked Data
gnomAD v4:
7-128858565-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128858565C>T , CM000669.2:g.128858565C>T | GRCh38 |
| NC_000007.13:g.128498619C>T , CM000669.1:g.128498619C>T | GRCh37 |
| NC_000007.12:g.128285855C>T | NCBI36 |
| NG_011807.1:g.33137C>T , LRG_870:g.33137C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.*42C>T (FLNC) MANE Select | ENSP00000327145.8:n.*42C>T | |
| ENST00000325888.12:c.*42C>T (FLNC) | ENSP00000327145.8:n.*42C>T | |
| ENST00000346177.6:c.*42C>T (FLNC) | ENSP00000344002.6:n.*42C>T | |
| NM_001127487.1:c.*42C>T (FLNC) | NP_001120959.1:n.*42C>T | |
| NM_001458.4:c.*42C>T , LRG_870t1:c.*42C>T (FLNC) | NP_001449.3:n.*42C>T | |
| NR_149055.1:n.102+3960G>A (FLNC-AS1) | ||
| NM_001127487.2:c.*42C>T (FLNC) | NP_001120959.1:n.*42C>T | |
| NM_001458.5:c.*42C>T (FLNC) MANE Select | NP_001449.3:n.*42C>T |