Canonical Allele Identifier: CA1742584513
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856670G= , CM000669.2:g.128856670G= GRCh38
NC_000007.13:g.128496724G= , CM000669.1:g.128496724G= GRCh37
NC_000007.12:g.128283960G= NCBI36
NG_011807.1:g.31242G= , LRG_870:g.31242G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7384+20G= (FLNC) MANE Select ENSP00000327145.8:n.7384+20G=
ENST00000325888.12:c.7384+20G= (FLNC) ENSP00000327145.8:n.7384+20G=
ENST00000346177.6:c.7285+20G= (FLNC) ENSP00000344002.6:n.7285+20G=
NM_001127487.1:c.7285+20G= (FLNC) NP_001120959.1:n.7285+20G=
NM_001458.4:c.7384+20G= , LRG_870t1:c.7384+20G= (FLNC) NP_001449.3:n.7384+20G=
NR_149055.1:n.103-3273C= (FLNC-AS1)
NM_001127487.2:c.7285+20G= (FLNC) NP_001120959.1:n.7285+20G=
NM_001458.5:c.7384+20G= (FLNC) MANE Select NP_001449.3:n.7384+20G=