Canonical Allele Identifier: CA369210984
Community Standard Title: NM_001458.5(FLNC):c.6031G>A (p.Gly2011Arg)
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852854G>A , CM000669.2:g.128852854G>A GRCh38
NC_000007.13:g.128492908G>A , CM000669.1:g.128492908G>A GRCh37
NC_000007.12:g.128280144G>A NCBI36
NG_011807.1:g.27426G>A , LRG_870:g.27426G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001458.5:c.6031G>A (FLNC) MANE Select NP_001449.3:p.Gly2011Arg
ENST00000325888.13:c.6031G>A (FLNC) MANE Select ENSP00000327145.8:p.Gly2011Arg
NM_001127487.1:c.5932G>A (FLNC) NP_001120959.1:p.Gly1978Arg
NM_001127487.2:c.5932G>A (FLNC) NP_001120959.1:p.Gly1978Arg
NM_001458.4:c.6031G>A , LRG_870t1:c.6031G>A (FLNC) NP_001449.3:p.Gly2011Arg
NR_149055.1:n.215+431C>T (FLNC-AS1)
ENST00000325888.12:c.6031G>A (FLNC) ENSP00000327145.8:p.Gly2011Arg
ENST00000346177.6:c.5932G>A (FLNC) ENSP00000344002.6:p.Gly1978Arg