Canonical Allele Identifier: CA4475799

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 472114
• ClinVar RCV Id: RCV000554648
• dbSNP Id: rs781168906
• ExAC: 7:128491690 G / A
• gnomAD v2: 7-128491690-G-A
• gnomAD v3: 7-128851636-G-A
• gnomAD v4: 7-128851636-G-A
• MyVariant Identifiers: chr7:g.128491690G>A (hg19) ; chr7:g.128851636G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128851636G>A , CM000669.2:g.128851636G>A	GRCh38
NC_000007.13:g.128491690G>A , CM000669.1:g.128491690G>A	GRCh37
NC_000007.12:g.128278926G>A	NCBI36
NG_011807.1:g.26208G>A , LRG_870:g.26208G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.5842+8G>A (FLNC) MANE Select	ENSP00000327145.8:n.5842+8G>A
ENST00000325888.12:c.5842+8G>A (FLNC)	ENSP00000327145.8:n.5842+8G>A
ENST00000346177.6:c.5743+8G>A (FLNC)	ENSP00000344002.6:n.5743+8G>A
NM_001127487.1:c.5743+8G>A (FLNC)	NP_001120959.1:n.5743+8G>A
NM_001458.4:c.5842+8G>A , LRG_870t1:c.5842+8G>A (FLNC)	NP_001449.3:n.5842+8G>A
NR_149055.1:n.216-136C>T (FLNC-AS1)
NM_001127487.2:c.5743+8G>A (FLNC)	NP_001120959.1:n.5743+8G>A
NM_001458.5:c.5842+8G>A (FLNC) MANE Select	NP_001449.3:n.5842+8G>A