Canonical Allele Identifier: CA2777853549
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853838_128853839insAAAC , CM000669.2:g.128853838_128853839insAAAC GRCh38
NC_000007.13:g.128493892_128493893insAAAC , CM000669.1:g.128493892_128493893insAAAC GRCh37
NC_000007.12:g.128281128_128281129insAAAC NCBI36
NG_011807.1:g.28410_28411insAAAC , LRG_870:g.28410_28411insAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6484+1_6484+2insAAAC (FLNC) MANE Select ENSP00000327145.8:n.6484+1_6484+2insAAAC
ENST00000325888.12:c.6484+1_6484+2insAAAC (FLNC) ENSP00000327145.8:n.6484+1_6484+2insAAAC
ENST00000346177.6:c.6385+1_6385+2insAAAC (FLNC) ENSP00000344002.6:n.6385+1_6385+2insAAAC
NM_001127487.1:c.6385+1_6385+2insAAAC (FLNC) NP_001120959.1:n.6385+1_6385+2insAAAC
NM_001458.4:c.6484+1_6484+2insAAAC , LRG_870t1:c.6484+1_6484+2insAAAC (FLNC) NP_001449.3:n.6484+1_6484+2insAAAC
NR_149055.1:n.103-442_103-441insGTTT (FLNC-AS1)
NM_001127487.2:c.6385+1_6385+2insAAAC (FLNC) NP_001120959.1:n.6385+1_6385+2insAAAC
NM_001458.5:c.6484+1_6484+2insAAAC (FLNC) MANE Select NP_001449.3:n.6484+1_6484+2insAAAC