Canonical Allele Identifier: CA1742584088
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856546C= , CM000669.2:g.128856546C= GRCh38
NC_000007.13:g.128496600C= , CM000669.1:g.128496600C= GRCh37
NC_000007.12:g.128283836C= NCBI36
NG_011807.1:g.31118C= , LRG_870:g.31118C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7280C= (FLNC) MANE Select ENSP00000327145.8:p.Ala2427=
ENST00000325888.12:c.7280C= (FLNC) ENSP00000327145.8:p.Ala2427=
ENST00000346177.6:c.7181C= (FLNC) ENSP00000344002.6:p.Ala2394=
NM_001127487.1:c.7181C= (FLNC) NP_001120959.1:p.Ala2394=
NM_001458.4:c.7280C= , LRG_870t1:c.7280C= (FLNC) NP_001449.3:p.Ala2427=
NR_149055.1:n.103-3149G= (FLNC-AS1)
NM_001127487.2:c.7181C= (FLNC) NP_001120959.1:p.Ala2394=
NM_001458.5:c.7280C= (FLNC) MANE Select NP_001449.3:p.Ala2427=