Canonical Allele Identifier: CA1742550558

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857362_128857379delinsACCCAGCCTGCAGCCCAG , CM000669.2:g.128857362_128857379delinsACCCAGCCTGCAGCCCAG	GRCh38
NC_000007.13:g.128497416_128497433delinsACCCAGCCTGCAGCCCAG , CM000669.1:g.128497416_128497433delinsACCCAGCCTGCAGCCCAG	GRCh37
NC_000007.12:g.128284652_128284669delinsACCCAGCCTGCAGCCCAG	NCBI36
NG_011807.1:g.31934_31951delinsACCCAGCCTGCAGCCCAG , LRG_870:g.31934_31951delinsACCCAGCCTGCAGCCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG (FLNC) MANE Select	ENSP00000327145.8:n.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG
ENST00000325888.12:c.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG (FLNC)	ENSP00000327145.8:n.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG
ENST00000346177.6:c.7681+26_7681+43delinsACCCAGCCTGCAGCCCAG (FLNC)	ENSP00000344002.6:n.7681+26_7681+43delinsACCCAGCCTGCAGCCCAG
NM_001127487.1:c.7681+26_7681+43delinsACCCAGCCTGCAGCCCAG (FLNC)	NP_001120959.1:n.7681+26_7681+43delinsACCCAGCCTGCAGCCCAG
NM_001458.4:c.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG , LRG_870t1:c.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG (FLNC)	NP_001449.3:n.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG
NR_149055.1:n.103-3982_103-3965delinsCTGGGCTGCAGGCTGGGT (FLNC-AS1)
NM_001127487.2:c.7681+26_7681+43delinsACCCAGCCTGCAGCCCAG (FLNC)	NP_001120959.1:n.7681+26_7681+43delinsACCCAGCCTGCAGCCCAG
NM_001458.5:c.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG (FLNC) MANE Select	NP_001449.3:n.7780+26_7780+43delinsACCCAGCCTGCAGCCCAG