Canonical Allele Identifier: CA457850401

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 539491
• ClinVar RCV Id: RCV000649232
• dbSNP Id: rs1490653520
• MyVariant Identifiers: chr7:g.128497269G>C (hg19) ; chr7:g.128857215G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857215G>C , CM000669.2:g.128857215G>C	GRCh38
NC_000007.13:g.128497269G>C , CM000669.1:g.128497269G>C	GRCh37
NC_000007.12:g.128284505G>C	NCBI36
NG_011807.1:g.31787G>C , LRG_870:g.31787G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7659G>C (FLNC) MANE Select	ENSP00000327145.8:p.Arg2553=
ENST00000325888.12:c.7659G>C (FLNC)	ENSP00000327145.8:p.Arg2553=
ENST00000346177.6:c.7560G>C (FLNC)	ENSP00000344002.6:p.Arg2520=
NM_001127487.1:c.7560G>C (FLNC)	NP_001120959.1:p.Arg2520=
NM_001458.4:c.7659G>C , LRG_870t1:c.7659G>C (FLNC)	NP_001449.3:p.Arg2553=
NR_149055.1:n.103-3818C>G (FLNC-AS1)
NM_001127487.2:c.7560G>C (FLNC)	NP_001120959.1:p.Arg2520=
NM_001458.5:c.7659G>C (FLNC) MANE Select	NP_001449.3:p.Arg2553=