Canonical Allele Identifier: CA2684820579

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128858169-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858169_128858170insGC , CM000669.2:g.128858169_128858170insGC	GRCh38
NC_000007.13:g.128498223_128498224insGC , CM000669.1:g.128498223_128498224insGC	GRCh37
NC_000007.12:g.128285459_128285460insGC	NCBI36
NG_011807.1:g.32741_32742insGC , LRG_870:g.32741_32742insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7942_7943insGC (FLNC) MANE Select	ENSP00000327145.8:p.Ala2648GlyfsTer21
ENST00000325888.12:c.7942_7943insGC (FLNC)	ENSP00000327145.8:p.Ala2648GlyfsTer21
ENST00000346177.6:c.7843_7844insGC (FLNC)	ENSP00000344002.6:p.Ala2615GlyfsTer21
NM_001127487.1:c.7843_7844insGC (FLNC)	NP_001120959.1:p.Ala2615GlyfsTer21
NM_001458.4:c.7942_7943insGC , LRG_870t1:c.7942_7943insGC (FLNC)	NP_001449.3:p.Ala2648GlyfsTer21
NR_149055.1:n.102+4355_102+4356insGC (FLNC-AS1)
NM_001127487.2:c.7843_7844insGC (FLNC)	NP_001120959.1:p.Ala2615GlyfsTer21
NM_001458.5:c.7942_7943insGC (FLNC) MANE Select	NP_001449.3:p.Ala2648GlyfsTer21