Canonical Allele Identifier: CA2684813289

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128852799-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128852799A>T , CM000669.2:g.128852799A>T	GRCh38
NC_000007.13:g.128492853A>T , CM000669.1:g.128492853A>T	GRCh37
NC_000007.12:g.128280089A>T	NCBI36
NG_011807.1:g.27371A>T , LRG_870:g.27371A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6005-29A>T (FLNC) MANE Select	ENSP00000327145.8:n.6005-29A>T
ENST00000325888.12:c.6005-29A>T (FLNC)	ENSP00000327145.8:n.6005-29A>T
ENST00000346177.6:c.5906-29A>T (FLNC)	ENSP00000344002.6:n.5906-29A>T
NM_001127487.1:c.5906-29A>T (FLNC)	NP_001120959.1:n.5906-29A>T
NM_001458.4:c.6005-29A>T , LRG_870t1:c.6005-29A>T (FLNC)	NP_001449.3:n.6005-29A>T
NR_149055.1:n.215+486T>A (FLNC-AS1)
NM_001127487.2:c.5906-29A>T (FLNC)	NP_001120959.1:n.5906-29A>T
NM_001458.5:c.6005-29A>T (FLNC) MANE Select	NP_001449.3:n.6005-29A>T