Canonical Allele Identifier: CA1742574385
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852560T= , CM000669.2:g.128852560T= GRCh38
NC_000007.13:g.128492614T= , CM000669.1:g.128492614T= GRCh37
NC_000007.12:g.128279850T= NCBI36
NG_011807.1:g.27132T= , LRG_870:g.27132T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5843-31T= (FLNC) MANE Select ENSP00000327145.8:n.5843-31T=
ENST00000325888.12:c.5843-31T= (FLNC) ENSP00000327145.8:n.5843-31T=
ENST00000346177.6:c.5744-31T= (FLNC) ENSP00000344002.6:n.5744-31T=
NM_001127487.1:c.5744-31T= (FLNC) NP_001120959.1:n.5744-31T=
NM_001458.4:c.5843-31T= , LRG_870t1:c.5843-31T= (FLNC) NP_001449.3:n.5843-31T=
NR_149055.1:n.215+725A= (FLNC-AS1)
NM_001127487.2:c.5744-31T= (FLNC) NP_001120959.1:n.5744-31T=
NM_001458.5:c.5843-31T= (FLNC) MANE Select NP_001449.3:n.5843-31T=