Canonical Allele Identifier: CA2684813850

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128853184-G-GGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853184_128853185insGCC , CM000669.2:g.128853184_128853185insGCC	GRCh38
NC_000007.13:g.128493238_128493239insGCC , CM000669.1:g.128493238_128493239insGCC	GRCh37
NC_000007.12:g.128280474_128280475insGCC	NCBI36
NG_011807.1:g.27756_27757insGCC , LRG_870:g.27756_27757insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6208+153_6208+154insGCC (FLNC) MANE Select	ENSP00000327145.8:n.6208+153_6208+154insGCC
ENST00000325888.12:c.6208+153_6208+154insGCC (FLNC)	ENSP00000327145.8:n.6208+153_6208+154insGCC
ENST00000346177.6:c.6109+153_6109+154insGCC (FLNC)	ENSP00000344002.6:n.6109+153_6109+154insGCC
NM_001127487.1:c.6109+153_6109+154insGCC (FLNC)	NP_001120959.1:n.6109+153_6109+154insGCC
NM_001458.4:c.6208+153_6208+154insGCC , LRG_870t1:c.6208+153_6208+154insGCC (FLNC)	NP_001449.3:n.6208+153_6208+154insGCC
NR_149055.1:n.215+100_215+101insGGC (FLNC-AS1)
NM_001127487.2:c.6109+153_6109+154insGCC (FLNC)	NP_001120959.1:n.6109+153_6109+154insGCC
NM_001458.5:c.6208+153_6208+154insGCC (FLNC) MANE Select	NP_001449.3:n.6208+153_6208+154insGCC