Canonical Allele Identifier: CA4476411
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 389112
ClinVar RCV Id: RCV001217767 RCV001698277 RCV002418316
dbSNP Id: rs369678123
ExAC: 7:128498412 C / T
gnomAD v2: 7-128498412-C-T
gnomAD v3: 7-128858358-C-T
gnomAD v4: 7-128858358-C-T
MyVariant Identifiers: chr7:g.128498412C>T (hg19) chr7:g.128858358C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858358C>T , CM000669.2:g.128858358C>T GRCh38
NC_000007.13:g.128498412C>T , CM000669.1:g.128498412C>T GRCh37
NC_000007.12:g.128285648C>T NCBI36
NG_011807.1:g.32930C>T , LRG_870:g.32930C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.8013C>T (FLNC) MANE Select ENSP00000327145.8:p.Gly2671=
ENST00000325888.12:c.8013C>T (FLNC) ENSP00000327145.8:p.Gly2671=
ENST00000346177.6:c.7914C>T (FLNC) ENSP00000344002.6:p.Gly2638=
NM_001127487.1:c.7914C>T (FLNC) NP_001120959.1:p.Gly2638=
NM_001458.4:c.8013C>T , LRG_870t1:c.8013C>T (FLNC) NP_001449.3:p.Gly2671=
NR_149055.1:n.102+4167G>A (FLNC-AS1)
NM_001127487.2:c.7914C>T (FLNC) NP_001120959.1:p.Gly2638=
NM_001458.5:c.8013C>T (FLNC) MANE Select NP_001449.3:p.Gly2671=
Search 100 bp 5'
Search 100 bp 3'