Canonical Allele Identifier: CA369220523

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 1062847
• ClinVar RCV Id: RCV001372611
• dbSNP Id: rs2128940603
• MyVariant Identifiers: chr7:g.128498212G>C (hg19) ; chr7:g.128858158G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858158G>C , CM000669.2:g.128858158G>C	GRCh38
NC_000007.13:g.128498212G>C , CM000669.1:g.128498212G>C	GRCh37
NC_000007.12:g.128285448G>C	NCBI36
NG_011807.1:g.32730G>C , LRG_870:g.32730G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7931G>C (FLNC) MANE Select	ENSP00000327145.8:p.Gly2644Ala
ENST00000325888.12:c.7931G>C (FLNC)	ENSP00000327145.8:p.Gly2644Ala
ENST00000346177.6:c.7832G>C (FLNC)	ENSP00000344002.6:p.Gly2611Ala
NM_001127487.1:c.7832G>C (FLNC)	NP_001120959.1:p.Gly2611Ala
NM_001458.4:c.7931G>C , LRG_870t1:c.7931G>C (FLNC)	NP_001449.3:p.Gly2644Ala
NR_149055.1:n.102+4367C>G (FLNC-AS1)
NM_001127487.2:c.7832G>C (FLNC)	NP_001120959.1:p.Gly2611Ala
NM_001458.5:c.7931G>C (FLNC) MANE Select	NP_001449.3:p.Gly2644Ala