Canonical Allele Identifier: CA1742549703
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856970C= , CM000669.2:g.128856970C= GRCh38
NC_000007.13:g.128497024C= , CM000669.1:g.128497024C= GRCh37
NC_000007.12:g.128284260C= NCBI36
NG_011807.1:g.31542C= , LRG_870:g.31542C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7561+49C= (FLNC) MANE Select ENSP00000327145.8:n.7561+49C=
ENST00000325888.12:c.7561+49C= (FLNC) ENSP00000327145.8:n.7561+49C=
ENST00000346177.6:c.7462+49C= (FLNC) ENSP00000344002.6:n.7462+49C=
NM_001127487.1:c.7462+49C= (FLNC) NP_001120959.1:n.7462+49C=
NM_001458.4:c.7561+49C= , LRG_870t1:c.7561+49C= (FLNC) NP_001449.3:n.7561+49C=
NR_149055.1:n.103-3573G= (FLNC-AS1)
NM_001127487.2:c.7462+49C= (FLNC) NP_001120959.1:n.7462+49C=
NM_001458.5:c.7561+49C= (FLNC) MANE Select NP_001449.3:n.7561+49C=