Canonical Allele Identifier: CA369208007

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 2942621
• ClinVar RCV Id: RCV003807787
• MyVariant Identifiers: chr7:g.128491527T>G (hg19) ; chr7:g.128851473T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128851473T>G , CM000669.2:g.128851473T>G	GRCh38
NC_000007.13:g.128491527T>G , CM000669.1:g.128491527T>G	GRCh37
NC_000007.12:g.128278763T>G	NCBI36
NG_011807.1:g.26045T>G , LRG_870:g.26045T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.5687T>G (FLNC) MANE Select	ENSP00000327145.8:p.Val1896Gly
ENST00000325888.12:c.5687T>G (FLNC)	ENSP00000327145.8:p.Val1896Gly
ENST00000346177.6:c.5588T>G (FLNC)	ENSP00000344002.6:p.Val1863Gly
NM_001127487.1:c.5588T>G (FLNC)	NP_001120959.1:p.Val1863Gly
NM_001458.4:c.5687T>G , LRG_870t1:c.5687T>G (FLNC)	NP_001449.3:p.Val1896Gly
NR_149055.1:n.243A>C (FLNC-AS1)
NM_001127487.2:c.5588T>G (FLNC)	NP_001120959.1:p.Val1863Gly
NM_001458.5:c.5687T>G (FLNC) MANE Select	NP_001449.3:p.Val1896Gly