Canonical Allele Identifier: CA2580610850
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 3068675
ClinVar RCV Id: RCV003994744
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847955del , CM000669.2:g.128847955del GRCh38
NC_000007.13:g.128488009del , CM000669.1:g.128488009del GRCh37
NC_000007.12:g.128275245del NCBI36
NG_011807.1:g.22527del , LRG_870:g.22527del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4467del MANE Select ENSP00000327145.8:p.Glu1489AspfsTer27
ENST00000325888.12:c.4467del ENSP00000327145.8:p.Glu1489AspfsTer27
ENST00000346177.6:c.4467del ENSP00000344002.6:p.Glu1489AspfsTer27
NM_001127487.1:c.4467del NP_001120959.1:p.Glu1489AspfsTer27
NM_001458.4:c.4467del , LRG_870t1:c.4467del NP_001449.3:p.Glu1489AspfsTer27
NM_001127487.2:c.4467del NP_001120959.1:p.Glu1489AspfsTer27
NM_001458.5:c.4467del MANE Select NP_001449.3:p.Glu1489AspfsTer27
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