Canonical Allele Identifier: CA1742579192
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854162T= , CM000669.2:g.128854162T= GRCh38
NC_000007.13:g.128494216T= , CM000669.1:g.128494216T= GRCh37
NC_000007.12:g.128281452T= NCBI36
NG_011807.1:g.28734T= , LRG_870:g.28734T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6673T= (FLNC) MANE Select ENSP00000327145.8:p.Phe2225=
ENST00000325888.12:c.6673T= (FLNC) ENSP00000327145.8:p.Phe2225=
ENST00000346177.6:c.6574T= (FLNC) ENSP00000344002.6:p.Phe2192=
NM_001127487.1:c.6574T= (FLNC) NP_001120959.1:p.Phe2192=
NM_001458.4:c.6673T= , LRG_870t1:c.6673T= (FLNC) NP_001449.3:p.Phe2225=
NR_149055.1:n.103-765A= (FLNC-AS1)
NM_001127487.2:c.6574T= (FLNC) NP_001120959.1:p.Phe2192=
NM_001458.5:c.6673T= (FLNC) MANE Select NP_001449.3:p.Phe2225=
Search 100 bp 5'
Search 100 bp 3'