Canonical Allele Identifier: CA1742577519
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853581C= , CM000669.2:g.128853581C= GRCh38
NC_000007.13:g.128493635C= , CM000669.1:g.128493635C= GRCh37
NC_000007.12:g.128280871C= NCBI36
NG_011807.1:g.28153C= , LRG_870:g.28153C=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6321C= (FLNC) MANE Select ENSP00000327145.8:p.Thr2107=
ENST00000325888.12:c.6321C= (FLNC) ENSP00000327145.8:p.Thr2107=
ENST00000346177.6:c.6222C= (FLNC) ENSP00000344002.6:p.Thr2074=
NM_001127487.1:c.6222C= (FLNC) NP_001120959.1:p.Thr2074=
NM_001458.4:c.6321C= , LRG_870t1:c.6321C= (FLNC) NP_001449.3:p.Thr2107=
NR_149055.1:n.103-184G= (FLNC-AS1)
NM_001127487.2:c.6222C= (FLNC) NP_001120959.1:p.Thr2074=
NM_001458.5:c.6321C= (FLNC) MANE Select NP_001449.3:p.Thr2107=
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Search 100 bp 3'