Linked Data
ClinVar Variation Id:
539341
ClinVar RCV Id:
RCV000649068
dbSNP Id:
rs773119692
ExAC:
7:128491420 G / A
gnomAD v2:
7-128491420-G-A
gnomAD v4:
7-128851366-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128851366G>A , CM000669.2:g.128851366G>A | GRCh38 |
| NC_000007.13:g.128491420G>A , CM000669.1:g.128491420G>A | GRCh37 |
| NC_000007.12:g.128278656G>A | NCBI36 |
| NG_011807.1:g.25938G>A , LRG_870:g.25938G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000325888.13:c.5668+6G>A (FLNC) MANE Select | ENSP00000327145.8:n.5668+6G>A | |
| ENST00000325888.12:c.5668+6G>A (FLNC) | ENSP00000327145.8:n.5668+6G>A | |
| ENST00000346177.6:c.5569+6G>A (FLNC) | ENSP00000344002.6:n.5569+6G>A | |
| NM_001127487.1:c.5569+6G>A (FLNC) | NP_001120959.1:n.5569+6G>A | |
| NM_001458.4:c.5668+6G>A , LRG_870t1:c.5668+6G>A (FLNC) | NP_001449.3:n.5668+6G>A | |
| NR_149055.1:n.315+35C>T (FLNC-AS1) | ||
| NM_001127487.2:c.5569+6G>A (FLNC) | NP_001120959.1:n.5569+6G>A | |
| NM_001458.5:c.5668+6G>A (FLNC) MANE Select | NP_001449.3:n.5668+6G>A |