Canonical Allele Identifier: CA2580076584
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1758581
ClinVar RCV Id: RCV002380377
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856640del , CM000669.2:g.128856640del GRCh38
NC_000007.13:g.128496694del , CM000669.1:g.128496694del GRCh37
NC_000007.12:g.128283930del NCBI36
NG_011807.1:g.31212del , LRG_870:g.31212del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7374del (FLNC) MANE Select ENSP00000327145.8:p.Glu2458AspfsTer?
ENST00000325888.12:c.7374del (FLNC) ENSP00000327145.8:p.Glu2458AspfsTer?
ENST00000346177.6:c.7275del (FLNC) ENSP00000344002.6:p.Glu2425AspfsTer?
NM_001127487.1:c.7275del (FLNC) NP_001120959.1:p.Glu2425AspfsTer?
NM_001458.4:c.7374del , LRG_870t1:c.7374del (FLNC) NP_001449.3:p.Glu2458AspfsTer?
NR_149055.1:n.103-3243del (FLNC-AS1)
NM_001127487.2:c.7275del (FLNC) NP_001120959.1:p.Glu2425AspfsTer?
NM_001458.5:c.7374del (FLNC) MANE Select NP_001449.3:p.Glu2458AspfsTer?
Search 100 bp 5'
Search 100 bp 3'