Canonical Allele Identifier: CA369220235

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 1492159
• ClinVar RCV Id: RCV001989187
• dbSNP Id: rs2128940583
• MyVariant Identifiers: chr7:g.128498145G>T (hg19) ; chr7:g.128858091G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858091G>T , CM000669.2:g.128858091G>T	GRCh38
NC_000007.13:g.128498145G>T , CM000669.1:g.128498145G>T	GRCh37
NC_000007.12:g.128285381G>T	NCBI36
NG_011807.1:g.32663G>T , LRG_870:g.32663G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7864G>T (FLNC) MANE Select	ENSP00000327145.8:p.Gly2622Cys
ENST00000325888.12:c.7864G>T (FLNC)	ENSP00000327145.8:p.Gly2622Cys
ENST00000346177.6:c.7765G>T (FLNC)	ENSP00000344002.6:p.Gly2589Cys
NM_001127487.1:c.7765G>T (FLNC)	NP_001120959.1:p.Gly2589Cys
NM_001458.4:c.7864G>T , LRG_870t1:c.7864G>T (FLNC)	NP_001449.3:p.Gly2622Cys
NR_149055.1:n.102+4434C>A (FLNC-AS1)
NM_001127487.2:c.7765G>T (FLNC)	NP_001120959.1:p.Gly2589Cys
NM_001458.5:c.7864G>T (FLNC) MANE Select	NP_001449.3:p.Gly2622Cys