Canonical Allele Identifier: CA166195207
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs979814571
gnomAD v4: 7-128857075-A-G
MyVariant Identifiers: chr7:g.128497129A>G (hg19) chr7:g.128857075A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857075A>G , CM000669.2:g.128857075A>G GRCh38
NC_000007.13:g.128497129A>G , CM000669.1:g.128497129A>G GRCh37
NC_000007.12:g.128284365A>G NCBI36
NG_011807.1:g.31647A>G , LRG_870:g.31647A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7562-43A>G (FLNC) MANE Select ENSP00000327145.8:n.7562-43A>G
ENST00000325888.12:c.7562-43A>G (FLNC) ENSP00000327145.8:n.7562-43A>G
ENST00000346177.6:c.7463-43A>G (FLNC) ENSP00000344002.6:n.7463-43A>G
NM_001127487.1:c.7463-43A>G (FLNC) NP_001120959.1:n.7463-43A>G
NM_001458.4:c.7562-43A>G , LRG_870t1:c.7562-43A>G (FLNC) NP_001449.3:n.7562-43A>G
NR_149055.1:n.103-3678T>C (FLNC-AS1)
NM_001127487.2:c.7463-43A>G (FLNC) NP_001120959.1:n.7463-43A>G
NM_001458.5:c.7562-43A>G (FLNC) MANE Select NP_001449.3:n.7562-43A>G
Search 100 bp 5'
Search 100 bp 3'