Canonical Allele Identifier: CA2684820741
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858601_128858602insC , CM000669.2:g.128858601_128858602insC GRCh38
NC_000007.13:g.128498655_128498656insC , CM000669.1:g.128498655_128498656insC GRCh37
NC_000007.12:g.128285891_128285892insC NCBI36
NG_011807.1:g.33173_33174insC , LRG_870:g.33173_33174insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*78_*79insC (FLNC) MANE Select ENSP00000327145.8:n.*78_*79insC
ENST00000325888.12:c.*78_*79insC (FLNC) ENSP00000327145.8:n.*78_*79insC
ENST00000346177.6:c.*78_*79insC (FLNC) ENSP00000344002.6:n.*78_*79insC
NM_001127487.1:c.*78_*79insC (FLNC) NP_001120959.1:n.*78_*79insC
NM_001458.4:c.*78_*79insC , LRG_870t1:c.*78_*79insC (FLNC) NP_001449.3:n.*78_*79insC
NR_149055.1:n.102+3923_102+3924insG (FLNC-AS1)
NM_001127487.2:c.*78_*79insC (FLNC) NP_001120959.1:n.*78_*79insC
NM_001458.5:c.*78_*79insC (FLNC) MANE Select NP_001449.3:n.*78_*79insC