Canonical Allele Identifier: CA1742575979
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852945C= , CM000669.2:g.128852945C= GRCh38
NC_000007.13:g.128492999C= , CM000669.1:g.128492999C= GRCh37
NC_000007.12:g.128280235C= NCBI36
NG_011807.1:g.27517C= , LRG_870:g.27517C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6122C= (FLNC) MANE Select ENSP00000327145.8:p.Ala2041=
ENST00000325888.12:c.6122C= (FLNC) ENSP00000327145.8:p.Ala2041=
ENST00000346177.6:c.6023C= (FLNC) ENSP00000344002.6:p.Ala2008=
NM_001127487.1:c.6023C= (FLNC) NP_001120959.1:p.Ala2008=
NM_001458.4:c.6122C= , LRG_870t1:c.6122C= (FLNC) NP_001449.3:p.Ala2041=
NR_149055.1:n.215+340G= (FLNC-AS1)
NM_001127487.2:c.6023C= (FLNC) NP_001120959.1:p.Ala2008=
NM_001458.5:c.6122C= (FLNC) MANE Select NP_001449.3:p.Ala2041=
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