Canonical Allele Identifier: CA2740094866

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 2941970
• ClinVar RCV Id: RCV003802992

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853025_128853042del , CM000669.2:g.128853025_128853042del	GRCh38
NC_000007.13:g.128493079_128493096del , CM000669.1:g.128493079_128493096del	GRCh37
NC_000007.12:g.128280315_128280332del	NCBI36
NG_011807.1:g.27597_27614del , LRG_870:g.27597_27614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6202_6208+11del (FLNC)
ENST00000325888.12:c.6202_6208+11del (FLNC)
ENST00000346177.6:c.6103_6109+11del (FLNC)
NM_001127487.1:c.6103_6109+11del (FLNC)
NM_001458.4:c.6202_6208+11del , LRG_870t1:c.6202_6208+11del (FLNC)
NR_149055.1:n.215+245_215+262del (FLNC-AS1)
NM_001127487.2:c.6103_6109+11del (FLNC)
NM_001458.5:c.6202_6208+11del (FLNC)