Canonical Allele Identifier: CA369221683

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 1413290
• ClinVar RCV Id: RCV001925829
• dbSNP Id: rs2128940675
• MyVariant Identifiers: chr7:g.128498486A>G (hg19) ; chr7:g.128858432A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858432A>G , CM000669.2:g.128858432A>G	GRCh38
NC_000007.13:g.128498486A>G , CM000669.1:g.128498486A>G	GRCh37
NC_000007.12:g.128285722A>G	NCBI36
NG_011807.1:g.33004A>G , LRG_870:g.33004A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.8087A>G (FLNC) MANE Select	ENSP00000327145.8:p.Tyr2696Cys
ENST00000325888.12:c.8087A>G (FLNC)	ENSP00000327145.8:p.Tyr2696Cys
ENST00000346177.6:c.7988A>G (FLNC)	ENSP00000344002.6:p.Tyr2663Cys
NM_001127487.1:c.7988A>G (FLNC)	NP_001120959.1:p.Tyr2663Cys
NM_001458.4:c.8087A>G , LRG_870t1:c.8087A>G (FLNC)	NP_001449.3:p.Tyr2696Cys
NR_149055.1:n.102+4093T>C (FLNC-AS1)
NM_001127487.2:c.7988A>G (FLNC)	NP_001120959.1:p.Tyr2663Cys
NM_001458.5:c.8087A>G (FLNC) MANE Select	NP_001449.3:p.Tyr2696Cys