Canonical Allele Identifier: CA369220227
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 650158
ClinVar RCV Id: RCV000805257
dbSNP Id: rs1411832198
gnomAD v2: 7-128498142-C-T
gnomAD v3: 7-128858088-C-T
gnomAD v4: 7-128858088-C-T
MyVariant Identifiers: chr7:g.128498142C>T (hg19) chr7:g.128858088C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858088C>T , CM000669.2:g.128858088C>T GRCh38
NC_000007.13:g.128498142C>T , CM000669.1:g.128498142C>T GRCh37
NC_000007.12:g.128285378C>T NCBI36
NG_011807.1:g.32660C>T , LRG_870:g.32660C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7861C>T (FLNC) MANE Select ENSP00000327145.8:p.Arg2621Trp
ENST00000325888.12:c.7861C>T (FLNC) ENSP00000327145.8:p.Arg2621Trp
ENST00000346177.6:c.7762C>T (FLNC) ENSP00000344002.6:p.Arg2588Trp
NM_001127487.1:c.7762C>T (FLNC) NP_001120959.1:p.Arg2588Trp
NM_001458.4:c.7861C>T , LRG_870t1:c.7861C>T (FLNC) NP_001449.3:p.Arg2621Trp
NR_149055.1:n.102+4437G>A (FLNC-AS1)
NM_001127487.2:c.7762C>T (FLNC) NP_001120959.1:p.Arg2588Trp
NM_001458.5:c.7861C>T (FLNC) MANE Select NP_001449.3:p.Arg2621Trp
Search 100 bp 5'
Search 100 bp 3'