Canonical Allele Identifier: CA1742578340
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853898G= , CM000669.2:g.128853898G= GRCh38
NC_000007.13:g.128493952G= , CM000669.1:g.128493952G= GRCh37
NC_000007.12:g.128281188G= NCBI36
NG_011807.1:g.28470G= , LRG_870:g.28470G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6484+61G= (FLNC) MANE Select ENSP00000327145.8:n.6484+61G=
ENST00000325888.12:c.6484+61G= (FLNC) ENSP00000327145.8:n.6484+61G=
ENST00000346177.6:c.6385+61G= (FLNC) ENSP00000344002.6:n.6385+61G=
NM_001127487.1:c.6385+61G= (FLNC) NP_001120959.1:n.6385+61G=
NM_001458.4:c.6484+61G= , LRG_870t1:c.6484+61G= (FLNC) NP_001449.3:n.6484+61G=
NR_149055.1:n.103-501C= (FLNC-AS1)
NM_001127487.2:c.6385+61G= (FLNC) NP_001120959.1:n.6385+61G=
NM_001458.5:c.6484+61G= (FLNC) MANE Select NP_001449.3:n.6484+61G=