Canonical Allele Identifier: CA4476424
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 752113
dbSNP Id: rs765388755

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858425G>A , CM000669.2:g.128858425G>A GRCh38
NC_000007.13:g.128498479G>A , CM000669.1:g.128498479G>A GRCh37
NC_000007.12:g.128285715G>A NCBI36
NG_011807.1:g.32997G>A , LRG_870:g.32997G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.8080G>A (FLNC) MANE Select ENSP00000327145.8:p.Val2694Ile
ENST00000325888.12:c.8080G>A (FLNC) ENSP00000327145.8:p.Val2694Ile
ENST00000346177.6:c.7981G>A (FLNC) ENSP00000344002.6:p.Val2661Ile
NM_001127487.1:c.7981G>A (FLNC) NP_001120959.1:p.Val2661Ile
NM_001458.4:c.8080G>A , LRG_870t1:c.8080G>A (FLNC) NP_001449.3:p.Val2694Ile
NR_149055.1:n.102+4100C>T (FLNC-AS1)
NM_001127487.2:c.7981G>A (FLNC) NP_001120959.1:p.Val2661Ile
NM_001458.5:c.8080G>A (FLNC) MANE Select NP_001449.3:p.Val2694Ile