Canonical Allele Identifier: CA4476373
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1017007
ClinVar RCV Id: RCV001316094 RCV002412014
dbSNP Id: rs745434129
ExAC: 7:128498121 G / A
gnomAD v2: 7-128498121-G-A
gnomAD v3: 7-128858067-G-A
gnomAD v4: 7-128858067-G-A
MyVariant Identifiers: chr7:g.128498121G>A (hg19) chr7:g.128858067G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858067G>A , CM000669.2:g.128858067G>A GRCh38
NC_000007.13:g.128498121G>A , CM000669.1:g.128498121G>A GRCh37
NC_000007.12:g.128285357G>A NCBI36
NG_011807.1:g.32639G>A , LRG_870:g.32639G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7840G>A (FLNC) MANE Select ENSP00000327145.8:p.Val2614Met
ENST00000325888.12:c.7840G>A (FLNC) ENSP00000327145.8:p.Val2614Met
ENST00000346177.6:c.7741G>A (FLNC) ENSP00000344002.6:p.Val2581Met
NM_001127487.1:c.7741G>A (FLNC) NP_001120959.1:p.Val2581Met
NM_001458.4:c.7840G>A , LRG_870t1:c.7840G>A (FLNC) NP_001449.3:p.Val2614Met
NR_149055.1:n.102+4458C>T (FLNC-AS1)
NM_001127487.2:c.7741G>A (FLNC) NP_001120959.1:p.Val2581Met
NM_001458.5:c.7840G>A (FLNC) MANE Select NP_001449.3:p.Val2614Met
Search 100 bp 5'
Search 100 bp 3'