Canonical Allele Identifier: CA891842996
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 567017
ClinVar RCV Id: RCV000686980 RCV003235349
dbSNP Id: rs1563001548
MyVariant Identifiers: chr7:g.128491512del (hg19) chr7:g.128851458del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851458del , CM000669.2:g.128851458del GRCh38
NC_000007.13:g.128491512del , CM000669.1:g.128491512del GRCh37
NC_000007.12:g.128278748del NCBI36
NG_011807.1:g.26030del , LRG_870:g.26030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5672del (FLNC)
ENST00000325888.12:c.5672del (FLNC)
ENST00000346177.6:c.5573del (FLNC)
NM_001127487.1:c.5573del (FLNC)
NM_001458.4:c.5672del , LRG_870t1:c.5672del (FLNC)
NR_149055.1:n.262del (FLNC-AS1)
NM_001127487.2:c.5573del (FLNC)
NM_001458.5:c.5672del (FLNC)
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