Canonical Allele Identifier: CA2579014564
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852816C>G , CM000669.2:g.128852816C>G GRCh38
NC_000007.13:g.128492870C>G , CM000669.1:g.128492870C>G GRCh37
NC_000007.12:g.128280106C>G NCBI36
NG_011807.1:g.27388C>G , LRG_870:g.27388C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6005-12C>G (FLNC) MANE Select ENSP00000327145.8:n.6005-12C>G
ENST00000325888.12:c.6005-12C>G (FLNC) ENSP00000327145.8:n.6005-12C>G
ENST00000346177.6:c.5906-12C>G (FLNC) ENSP00000344002.6:n.5906-12C>G
NM_001127487.1:c.5906-12C>G (FLNC) NP_001120959.1:n.5906-12C>G
NM_001458.4:c.6005-12C>G , LRG_870t1:c.6005-12C>G (FLNC) NP_001449.3:n.6005-12C>G
NR_149055.1:n.215+469G>C (FLNC-AS1)
NM_001127487.2:c.5906-12C>G (FLNC) NP_001120959.1:n.5906-12C>G
NM_001458.5:c.6005-12C>G (FLNC) MANE Select NP_001449.3:n.6005-12C>G