Canonical Allele Identifier: CA915945514
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 755194
ClinVar RCV Id: RCV001498484
dbSNP Id: rs1585167904
gnomAD v4: 7-128852821-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852821T>C , CM000669.2:g.128852821T>C GRCh38
NC_000007.13:g.128492875T>C , CM000669.1:g.128492875T>C GRCh37
NC_000007.12:g.128280111T>C NCBI36
NG_011807.1:g.27393T>C , LRG_870:g.27393T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6005-7T>C (FLNC) MANE Select ENSP00000327145.8:n.6005-7T>C
ENST00000325888.12:c.6005-7T>C (FLNC) ENSP00000327145.8:n.6005-7T>C
ENST00000346177.6:c.5906-7T>C (FLNC) ENSP00000344002.6:n.5906-7T>C
NM_001127487.1:c.5906-7T>C (FLNC) NP_001120959.1:n.5906-7T>C
NM_001458.4:c.6005-7T>C , LRG_870t1:c.6005-7T>C (FLNC) NP_001449.3:n.6005-7T>C
NR_149055.1:n.215+464A>G (FLNC-AS1)
NM_001127487.2:c.5906-7T>C (FLNC) NP_001120959.1:n.5906-7T>C
NM_001458.5:c.6005-7T>C (FLNC) MANE Select NP_001449.3:n.6005-7T>C
Search 100 bp 5'
Search 100 bp 3'