Canonical Allele Identifier: CA2684820625
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128858316-C-CCCTCTG
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858321_128858326dup , CM000669.2:g.128858321_128858326dup GRCh38
NC_000007.13:g.128498375_128498380dup , CM000669.1:g.128498375_128498380dup GRCh37
NC_000007.12:g.128285611_128285616dup NCBI36
NG_011807.1:g.32893_32898dup , LRG_870:g.32893_32898dup

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7991-15_7991-10dup (FLNC) MANE Select ENSP00000327145.8:n.7991-15_7991-10dup
ENST00000325888.12:c.7991-15_7991-10dup (FLNC) ENSP00000327145.8:n.7991-15_7991-10dup
ENST00000346177.6:c.7892-15_7892-10dup (FLNC) ENSP00000344002.6:n.7892-15_7892-10dup
NM_001127487.1:c.7892-15_7892-10dup (FLNC) NP_001120959.1:n.7892-15_7892-10dup
NM_001458.4:c.7991-15_7991-10dup , LRG_870t1:c.7991-15_7991-10dup (FLNC) NP_001449.3:n.7991-15_7991-10dup
NR_149055.1:n.102+4203_102+4208dup (FLNC-AS1)
NM_001127487.2:c.7892-15_7892-10dup (FLNC) NP_001120959.1:n.7892-15_7892-10dup
NM_001458.5:c.7991-15_7991-10dup (FLNC) MANE Select NP_001449.3:n.7991-15_7991-10dup
Search 100 bp 5'
Search 100 bp 3'