Canonical Allele Identifier: CA4475869
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 573927
ClinVar RCV Id: RCV000695729
dbSNP Id: rs747796553

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852828G>T , CM000669.2:g.128852828G>T GRCh38
NC_000007.13:g.128492882G>T , CM000669.1:g.128492882G>T GRCh37
NC_000007.12:g.128280118G>T NCBI36
NG_011807.1:g.27400G>T , LRG_870:g.27400G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6005G>T (FLNC) MANE Select ENSP00000327145.8:p.Gly2002Val
ENST00000325888.12:c.6005G>T (FLNC) ENSP00000327145.8:p.Gly2002Val
ENST00000346177.6:c.5906G>T (FLNC) ENSP00000344002.6:p.Gly1969Val
NM_001127487.1:c.5906G>T (FLNC) NP_001120959.1:p.Gly1969Val
NM_001458.4:c.6005G>T , LRG_870t1:c.6005G>T (FLNC) NP_001449.3:p.Gly2002Val
NR_149055.1:n.215+457C>A (FLNC-AS1)
NM_001127487.2:c.5906G>T (FLNC) NP_001120959.1:p.Gly1969Val
NM_001458.5:c.6005G>T (FLNC) MANE Select NP_001449.3:p.Gly2002Val