Canonical Allele Identifier: CA166193551
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 539346
dbSNP Id: rs376257910

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128855285G>A , CM000669.2:g.128855285G>A GRCh38
NC_000007.13:g.128495339G>A , CM000669.1:g.128495339G>A GRCh37
NC_000007.12:g.128282575G>A NCBI36
NG_011807.1:g.29857G>A , LRG_870:g.29857G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7222G>A (FLNC) MANE Select ENSP00000327145.8:p.Ala2408Thr
ENST00000325888.12:c.7222G>A (FLNC) ENSP00000327145.8:p.Ala2408Thr
ENST00000346177.6:c.7123G>A (FLNC) ENSP00000344002.6:p.Ala2375Thr
NM_001127487.1:c.7123G>A (FLNC) NP_001120959.1:p.Ala2375Thr
NM_001458.4:c.7222G>A , LRG_870t1:c.7222G>A (FLNC) NP_001449.3:p.Ala2408Thr
NR_149055.1:n.103-1888C>T (FLNC-AS1)
NM_001127487.2:c.7123G>A (FLNC) NP_001120959.1:p.Ala2375Thr
NM_001458.5:c.7222G>A (FLNC) MANE Select NP_001449.3:p.Ala2408Thr