Canonical Allele Identifier: CA2579014630
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854691C>A , CM000669.2:g.128854691C>A GRCh38
NC_000007.13:g.128494745C>A , CM000669.1:g.128494745C>A GRCh37
NC_000007.12:g.128281981C>A NCBI36
NG_011807.1:g.29263C>A , LRG_870:g.29263C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6997+9C>A (FLNC) MANE Select ENSP00000327145.8:n.6997+9C>A
ENST00000325888.12:c.6997+9C>A (FLNC) ENSP00000327145.8:n.6997+9C>A
ENST00000346177.6:c.6898+9C>A (FLNC) ENSP00000344002.6:n.6898+9C>A
NM_001127487.1:c.6898+9C>A (FLNC) NP_001120959.1:n.6898+9C>A
NM_001458.4:c.6997+9C>A , LRG_870t1:c.6997+9C>A (FLNC) NP_001449.3:n.6997+9C>A
NR_149055.1:n.103-1294G>T (FLNC-AS1)
NM_001127487.2:c.6898+9C>A (FLNC) NP_001120959.1:n.6898+9C>A
NM_001458.5:c.6997+9C>A (FLNC) MANE Select NP_001449.3:n.6997+9C>A