Canonical Allele Identifier: CA2684820794
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128858642-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858642C>A , CM000669.2:g.128858642C>A GRCh38
NC_000007.13:g.128498696C>A , CM000669.1:g.128498696C>A GRCh37
NC_000007.12:g.128285932C>A NCBI36
NG_011807.1:g.33214C>A , LRG_870:g.33214C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*119C>A (FLNC) MANE Select ENSP00000327145.8:n.*119C>A
ENST00000325888.12:c.*119C>A (FLNC) ENSP00000327145.8:n.*119C>A
ENST00000346177.6:c.*119C>A (FLNC) ENSP00000344002.6:n.*119C>A
NM_001127487.1:c.*119C>A (FLNC) NP_001120959.1:n.*119C>A
NM_001458.4:c.*119C>A , LRG_870t1:c.*119C>A (FLNC) NP_001449.3:n.*119C>A
NR_149055.1:n.102+3883G>T (FLNC-AS1)
NM_001127487.2:c.*119C>A (FLNC) NP_001120959.1:n.*119C>A
NM_001458.5:c.*119C>A (FLNC) MANE Select NP_001449.3:n.*119C>A
Search 100 bp 5'
Search 100 bp 3'