Canonical Allele Identifier: CA913189350
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 599235
ClinVar RCV Id: RCV000735825
dbSNP Id: rs1563005360
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857103_128857193delinsGAGG , CM000669.2:g.128857103_128857193delinsGAGG GRCh38
NC_000007.13:g.128497157_128497247delinsGAGG , CM000669.1:g.128497157_128497247delinsGAGG GRCh37
NC_000007.12:g.128284393_128284483delinsGAGG NCBI36
NG_011807.1:g.31675_31765delinsGAGG , LRG_870:g.31675_31765delinsGAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7562-15_7637delinsGAGG (FLNC)
ENST00000325888.12:c.7562-15_7637delinsGAGG (FLNC)
ENST00000346177.6:c.7463-15_7538delinsGAGG (FLNC)
NM_001127487.1:c.7463-15_7538delinsGAGG (FLNC)
NM_001458.4:c.7562-15_7637delinsGAGG , LRG_870t1:c.7562-15_7637delinsGAGG (FLNC)
NR_149055.1:n.103-3796_103-3706delinsCCTC (FLNC-AS1)
NM_001127487.2:c.7463-15_7538delinsGAGG (FLNC)
NM_001458.5:c.7562-15_7637delinsGAGG (FLNC)
Search 100 bp 5'
Search 100 bp 3'