Canonical Allele Identifier: CA1742578388

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853923_128853924delinsCT , CM000669.2:g.128853923_128853924delinsCT	GRCh38
NC_000007.13:g.128493977_128493978delinsCT , CM000669.1:g.128493977_128493978delinsCT	GRCh37
NC_000007.12:g.128281213_128281214delinsCT	NCBI36
NG_011807.1:g.28495_28496delinsCT , LRG_870:g.28495_28496delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6485-51_6485-50delinsCT (FLNC) MANE Select	ENSP00000327145.8:n.6485-51_6485-50delinsCT
ENST00000325888.12:c.6485-51_6485-50delinsCT (FLNC)	ENSP00000327145.8:n.6485-51_6485-50delinsCT
ENST00000346177.6:c.6386-51_6386-50delinsCT (FLNC)	ENSP00000344002.6:n.6386-51_6386-50delinsCT
NM_001127487.1:c.6386-51_6386-50delinsCT (FLNC)	NP_001120959.1:n.6386-51_6386-50delinsCT
NM_001458.4:c.6485-51_6485-50delinsCT , LRG_870t1:c.6485-51_6485-50delinsCT (FLNC)	NP_001449.3:n.6485-51_6485-50delinsCT
NR_149055.1:n.103-527_103-526delinsAG (FLNC-AS1)
NM_001127487.2:c.6386-51_6386-50delinsCT (FLNC)	NP_001120959.1:n.6386-51_6386-50delinsCT
NM_001458.5:c.6485-51_6485-50delinsCT (FLNC) MANE Select	NP_001449.3:n.6485-51_6485-50delinsCT