Canonical Allele Identifier: CA457590387
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 472174
ClinVar RCV Id: RCV000550977
dbSNP Id: rs1554401819

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856815C>G , CM000669.2:g.128856815C>G GRCh38
NC_000007.13:g.128496869C>G , CM000669.1:g.128496869C>G GRCh37
NC_000007.12:g.128284105C>G NCBI36
NG_011807.1:g.31387C>G , LRG_870:g.31387C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7455C>G (FLNC) MANE Select ENSP00000327145.8:p.Ala2485=
ENST00000325888.12:c.7455C>G (FLNC) ENSP00000327145.8:p.Ala2485=
ENST00000346177.6:c.7356C>G (FLNC) ENSP00000344002.6:p.Ala2452=
NM_001127487.1:c.7356C>G (FLNC) NP_001120959.1:p.Ala2452=
NM_001458.4:c.7455C>G , LRG_870t1:c.7455C>G (FLNC) NP_001449.3:p.Ala2485=
NR_149055.1:n.103-3418G>C (FLNC-AS1)
NM_001127487.2:c.7356C>G (FLNC) NP_001120959.1:p.Ala2452=
NM_001458.5:c.7455C>G (FLNC) MANE Select NP_001449.3:p.Ala2485=