Canonical Allele Identifier: CA2684813722

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128853137-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853137T>C , CM000669.2:g.128853137T>C	GRCh38
NC_000007.13:g.128493191T>C , CM000669.1:g.128493191T>C	GRCh37
NC_000007.12:g.128280427T>C	NCBI36
NG_011807.1:g.27709T>C , LRG_870:g.27709T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6208+106T>C (FLNC) MANE Select	ENSP00000327145.8:n.6208+106T>C
ENST00000325888.12:c.6208+106T>C (FLNC)	ENSP00000327145.8:n.6208+106T>C
ENST00000346177.6:c.6109+106T>C (FLNC)	ENSP00000344002.6:n.6109+106T>C
NM_001127487.1:c.6109+106T>C (FLNC)	NP_001120959.1:n.6109+106T>C
NM_001458.4:c.6208+106T>C , LRG_870t1:c.6208+106T>C (FLNC)	NP_001449.3:n.6208+106T>C
NR_149055.1:n.215+148A>G (FLNC-AS1)
NM_001127487.2:c.6109+106T>C (FLNC)	NP_001120959.1:n.6109+106T>C
NM_001458.5:c.6208+106T>C (FLNC) MANE Select	NP_001449.3:n.6208+106T>C