Canonical Allele Identifier: CA1742589520

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128848015_128848017delinsTGA , CM000669.2:g.128848015_128848017delinsTGA	GRCh38
NC_000007.13:g.128488069_128488071delinsTGA , CM000669.1:g.128488069_128488071delinsTGA	GRCh37
NC_000007.12:g.128275305_128275307delinsTGA	NCBI36
NG_011807.1:g.22587_22589delinsTGA , LRG_870:g.22587_22589delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4527_4529delinsTGA MANE Select	ENSP00000327145.8:p.Thr1509=
ENST00000325888.12:c.4527_4529delinsTGA	ENSP00000327145.8:p.Thr1509=
ENST00000346177.6:c.4527_4529delinsTGA	ENSP00000344002.6:p.Thr1509=
NM_001127487.1:c.4527_4529delinsTGA	NP_001120959.1:p.Thr1509=
NM_001458.4:c.4527_4529delinsTGA , LRG_870t1:c.4527_4529delinsTGA	NP_001449.3:p.Thr1509=
NM_001127487.2:c.4527_4529delinsTGA	NP_001120959.1:p.Thr1509=
NM_001458.5:c.4527_4529delinsTGA MANE Select	NP_001449.3:p.Thr1509=