Canonical Allele Identifier: CA369212735

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 2939300
• ClinVar RCV Id: RCV003792026
• MyVariant Identifiers: chr7:g.128494060C>A (hg19) ; chr7:g.128854006C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128854006C>A , CM000669.2:g.128854006C>A	GRCh38
NC_000007.13:g.128494060C>A , CM000669.1:g.128494060C>A	GRCh37
NC_000007.12:g.128281296C>A	NCBI36
NG_011807.1:g.28578C>A , LRG_870:g.28578C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6517C>A (FLNC) MANE Select	ENSP00000327145.8:p.Arg2173Ser
ENST00000325888.12:c.6517C>A (FLNC)	ENSP00000327145.8:p.Arg2173Ser
ENST00000346177.6:c.6418C>A (FLNC)	ENSP00000344002.6:p.Arg2140Ser
NM_001127487.1:c.6418C>A (FLNC)	NP_001120959.1:p.Arg2140Ser
NM_001458.4:c.6517C>A , LRG_870t1:c.6517C>A (FLNC)	NP_001449.3:p.Arg2173Ser
NR_149055.1:n.103-609G>T (FLNC-AS1)
NM_001127487.2:c.6418C>A (FLNC)	NP_001120959.1:p.Arg2140Ser
NM_001458.5:c.6517C>A (FLNC) MANE Select	NP_001449.3:p.Arg2173Ser