Canonical Allele Identifier: CA369208492
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808816681

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851585T>A , CM000669.2:g.128851585T>A GRCh38
NC_000007.13:g.128491639T>A , CM000669.1:g.128491639T>A GRCh37
NC_000007.12:g.128278875T>A NCBI36
NG_011807.1:g.26157T>A , LRG_870:g.26157T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5799T>A (FLNC) MANE Select ENSP00000327145.8:p.Asp1933Glu
ENST00000325888.12:c.5799T>A (FLNC) ENSP00000327145.8:p.Asp1933Glu
ENST00000346177.6:c.5700T>A (FLNC) ENSP00000344002.6:p.Asp1900Glu
NM_001127487.1:c.5700T>A (FLNC) NP_001120959.1:p.Asp1900Glu
NM_001458.4:c.5799T>A , LRG_870t1:c.5799T>A (FLNC) NP_001449.3:p.Asp1933Glu
NR_149055.1:n.216-85A>T (FLNC-AS1)
NM_001127487.2:c.5700T>A (FLNC) NP_001120959.1:p.Asp1900Glu
NM_001458.5:c.5799T>A (FLNC) MANE Select NP_001449.3:p.Asp1933Glu