Canonical Allele Identifier: CA166195404

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 576606
• ClinVar RCV Id: RCV000699140 ; RCV000998925 ; RCV002388294
• dbSNP Id: rs777724201
• gnomAD v2: 7-128497215-G-A
• gnomAD v3: 7-128857161-G-A
• gnomAD v4: 7-128857161-G-A
• MyVariant Identifiers: chr7:g.128497215G>A (hg19) ; chr7:g.128857161G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857161G>A , CM000669.2:g.128857161G>A	GRCh38
NC_000007.13:g.128497215G>A , CM000669.1:g.128497215G>A	GRCh37
NC_000007.12:g.128284451G>A	NCBI36
NG_011807.1:g.31733G>A , LRG_870:g.31733G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7605G>A (FLNC) MANE Select	ENSP00000327145.8:p.Ser2535=
ENST00000325888.12:c.7605G>A (FLNC)	ENSP00000327145.8:p.Ser2535=
ENST00000346177.6:c.7506G>A (FLNC)	ENSP00000344002.6:p.Ser2502=
NM_001127487.1:c.7506G>A (FLNC)	NP_001120959.1:p.Ser2502=
NM_001458.4:c.7605G>A , LRG_870t1:c.7605G>A (FLNC)	NP_001449.3:p.Ser2535=
NR_149055.1:n.103-3764C>T (FLNC-AS1)
NM_001127487.2:c.7506G>A (FLNC)	NP_001120959.1:p.Ser2502=
NM_001458.5:c.7605G>A (FLNC) MANE Select	NP_001449.3:p.Ser2535=