Canonical Allele Identifier: CA1742571484
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851568A= , CM000669.2:g.128851568A= GRCh38
NC_000007.13:g.128491622A= , CM000669.1:g.128491622A= GRCh37
NC_000007.12:g.128278858A= NCBI36
NG_011807.1:g.26140A= , LRG_870:g.26140A=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5782A= (FLNC) MANE Select ENSP00000327145.8:p.Ile1928=
ENST00000325888.12:c.5782A= (FLNC) ENSP00000327145.8:p.Ile1928=
ENST00000346177.6:c.5683A= (FLNC) ENSP00000344002.6:p.Ile1895=
NM_001127487.1:c.5683A= (FLNC) NP_001120959.1:p.Ile1895=
NM_001458.4:c.5782A= , LRG_870t1:c.5782A= (FLNC) NP_001449.3:p.Ile1928=
NR_149055.1:n.216-68T= (FLNC-AS1)
NM_001127487.2:c.5683A= (FLNC) NP_001120959.1:p.Ile1895=
NM_001458.5:c.5782A= (FLNC) MANE Select NP_001449.3:p.Ile1928=