Canonical Allele Identifier: CA1742578444
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853971C= , CM000669.2:g.128853971C= GRCh38
NC_000007.13:g.128494025C= , CM000669.1:g.128494025C= GRCh37
NC_000007.12:g.128281261C= NCBI36
NG_011807.1:g.28543C= , LRG_870:g.28543C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6485-3C= (FLNC) MANE Select ENSP00000327145.8:n.6485-3C=
ENST00000325888.12:c.6485-3C= (FLNC) ENSP00000327145.8:n.6485-3C=
ENST00000346177.6:c.6386-3C= (FLNC) ENSP00000344002.6:n.6386-3C=
NM_001127487.1:c.6386-3C= (FLNC) NP_001120959.1:n.6386-3C=
NM_001458.4:c.6485-3C= , LRG_870t1:c.6485-3C= (FLNC) NP_001449.3:n.6485-3C=
NR_149055.1:n.103-574G= (FLNC-AS1)
NM_001127487.2:c.6386-3C= (FLNC) NP_001120959.1:n.6386-3C=
NM_001458.5:c.6485-3C= (FLNC) MANE Select NP_001449.3:n.6485-3C=