Canonical Allele Identifier: CA2684820727

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128858597-A-ACACG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858599_128858600insCGCA , CM000669.2:g.128858599_128858600insCGCA	GRCh38
NC_000007.13:g.128498653_128498654insCGCA , CM000669.1:g.128498653_128498654insCGCA	GRCh37
NC_000007.12:g.128285889_128285890insCGCA	NCBI36
NG_011807.1:g.33171_33172insCGCA , LRG_870:g.33171_33172insCGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.*76_*77insCGCA (FLNC) MANE Select	ENSP00000327145.8:n.*76_*77insCGCA
ENST00000325888.12:c.*76_*77insCGCA (FLNC)	ENSP00000327145.8:n.*76_*77insCGCA
ENST00000346177.6:c.*76_*77insCGCA (FLNC)	ENSP00000344002.6:n.*76_*77insCGCA
NM_001127487.1:c.*76_*77insCGCA (FLNC)	NP_001120959.1:n.*76_*77insCGCA
NM_001458.4:c.*76_*77insCGCA , LRG_870t1:c.*76_*77insCGCA (FLNC)	NP_001449.3:n.*76_*77insCGCA
NR_149055.1:n.102+3927_102+3928insCGTG (FLNC-AS1)
NM_001127487.2:c.*76_*77insCGCA (FLNC)	NP_001120959.1:n.*76_*77insCGCA
NM_001458.5:c.*76_*77insCGCA (FLNC) MANE Select	NP_001449.3:n.*76_*77insCGCA