Canonical Allele Identifier: CA369221917
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 860247
ClinVar RCV Id: RCV001066522
dbSNP Id: rs28437296

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858466T>G , CM000669.2:g.128858466T>G GRCh38
NC_000007.13:g.128498520T>G , CM000669.1:g.128498520T>G GRCh37
NC_000007.12:g.128285756T>G NCBI36
NG_011807.1:g.33038T>G , LRG_870:g.33038T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.8121T>G (FLNC) MANE Select ENSP00000327145.8:p.Ile2707Met
ENST00000325888.12:c.8121T>G (FLNC) ENSP00000327145.8:p.Ile2707Met
ENST00000346177.6:c.8022T>G (FLNC) ENSP00000344002.6:p.Ile2674Met
NM_001127487.1:c.8022T>G (FLNC) NP_001120959.1:p.Ile2674Met
NM_001458.4:c.8121T>G , LRG_870t1:c.8121T>G (FLNC) NP_001449.3:p.Ile2707Met
NR_149055.1:n.102+4059A>C (FLNC-AS1)
NM_001127487.2:c.8022T>G (FLNC) NP_001120959.1:p.Ile2674Met
NM_001458.5:c.8121T>G (FLNC) MANE Select NP_001449.3:p.Ile2707Met