Canonical Allele Identifier: CA4476237
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 472168
dbSNP Id: rs370293647

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856594G>A , CM000669.2:g.128856594G>A GRCh38
NC_000007.13:g.128496648G>A , CM000669.1:g.128496648G>A GRCh37
NC_000007.12:g.128283884G>A NCBI36
NG_011807.1:g.31166G>A , LRG_870:g.31166G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7328G>A (FLNC) MANE Select ENSP00000327145.8:p.Arg2443Gln
ENST00000325888.12:c.7328G>A (FLNC) ENSP00000327145.8:p.Arg2443Gln
ENST00000346177.6:c.7229G>A (FLNC) ENSP00000344002.6:p.Arg2410Gln
NM_001127487.1:c.7229G>A (FLNC) NP_001120959.1:p.Arg2410Gln
NM_001458.4:c.7328G>A , LRG_870t1:c.7328G>A (FLNC) NP_001449.3:p.Arg2443Gln
NR_149055.1:n.103-3197C>T (FLNC-AS1)
NM_001127487.2:c.7229G>A (FLNC) NP_001120959.1:p.Arg2410Gln
NM_001458.5:c.7328G>A (FLNC) MANE Select NP_001449.3:p.Arg2443Gln