Linked Data
ClinVar Variation Id:
539511
ClinVar RCV Id:
RCV000649254
dbSNP Id:
rs1032374300
gnomAD v2:
7-128498111-G-C
gnomAD v3:
7-128858057-G-C
gnomAD v4:
7-128858057-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128858057G>C , CM000669.2:g.128858057G>C | GRCh38 |
| NC_000007.13:g.128498111G>C , CM000669.1:g.128498111G>C | GRCh37 |
| NC_000007.12:g.128285347G>C | NCBI36 |
| NG_011807.1:g.32629G>C , LRG_870:g.32629G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.7830G>C (FLNC) MANE Select | ENSP00000327145.8:p.Leu2610= | |
| ENST00000325888.12:c.7830G>C (FLNC) | ENSP00000327145.8:p.Leu2610= | |
| ENST00000346177.6:c.7731G>C (FLNC) | ENSP00000344002.6:p.Leu2577= | |
| NM_001127487.1:c.7731G>C (FLNC) | NP_001120959.1:p.Leu2577= | |
| NM_001458.4:c.7830G>C , LRG_870t1:c.7830G>C (FLNC) | NP_001449.3:p.Leu2610= | |
| NR_149055.1:n.102+4468C>G (FLNC-AS1) | ||
| NM_001127487.2:c.7731G>C (FLNC) | NP_001120959.1:p.Leu2577= | |
| NM_001458.5:c.7830G>C (FLNC) MANE Select | NP_001449.3:p.Leu2610= |