Canonical Allele Identifier: CA1742552041
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858319T= , CM000669.2:g.128858319T= GRCh38
NC_000007.13:g.128498373T= , CM000669.1:g.128498373T= GRCh37
NC_000007.12:g.128285609T= NCBI36
NG_011807.1:g.32891T= , LRG_870:g.32891T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7991-17T= (FLNC) MANE Select ENSP00000327145.8:n.7991-17T=
ENST00000325888.12:c.7991-17T= (FLNC) ENSP00000327145.8:n.7991-17T=
ENST00000346177.6:c.7892-17T= (FLNC) ENSP00000344002.6:n.7892-17T=
NM_001127487.1:c.7892-17T= (FLNC) NP_001120959.1:n.7892-17T=
NM_001458.4:c.7991-17T= , LRG_870t1:c.7991-17T= (FLNC) NP_001449.3:n.7991-17T=
NR_149055.1:n.102+4206A= (FLNC-AS1)
NM_001127487.2:c.7892-17T= (FLNC) NP_001120959.1:n.7892-17T=
NM_001458.5:c.7991-17T= (FLNC) MANE Select NP_001449.3:n.7991-17T=
Search 100 bp 5'
Search 100 bp 3'