Linked Data
ClinVar Variation Id:
383328
dbSNP Id:
rs116974302
ExAC:
7:128492997 C / T
gnomAD v2:
7-128492997-C-T
gnomAD v3:
7-128852943-C-T
gnomAD v4:
7-128852943-C-T
COSMIC:
COSM3784979
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128852943C>T , CM000669.2:g.128852943C>T | GRCh38 |
| NC_000007.13:g.128492997C>T , CM000669.1:g.128492997C>T | GRCh37 |
| NC_000007.12:g.128280233C>T | NCBI36 |
| NG_011807.1:g.27515C>T , LRG_870:g.27515C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000325888.13:c.6120C>T (FLNC) MANE Select | ENSP00000327145.8:p.Asp2040= | |
| ENST00000325888.12:c.6120C>T (FLNC) | ENSP00000327145.8:p.Asp2040= | |
| ENST00000346177.6:c.6021C>T (FLNC) | ENSP00000344002.6:p.Asp2007= | |
| NM_001127487.1:c.6021C>T (FLNC) | NP_001120959.1:p.Asp2007= | |
| NM_001458.4:c.6120C>T , LRG_870t1:c.6120C>T (FLNC) | NP_001449.3:p.Asp2040= | |
| NR_149055.1:n.215+342G>A (FLNC-AS1) | ||
| NM_001127487.2:c.6021C>T (FLNC) | NP_001120959.1:p.Asp2007= | |
| NM_001458.5:c.6120C>T (FLNC) MANE Select | NP_001449.3:p.Asp2040= |