Canonical Allele Identifier: CA369219719
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2923718
ClinVar RCV Id: RCV003783276
dbSNP Id: rs1421296226
gnomAD v2: 7-128497307-T-C
gnomAD v3: 7-128857253-T-C
gnomAD v4: 7-128857253-T-C
MyVariant Identifiers: chr7:g.128497307T>C (hg19) chr7:g.128857253T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857253T>C , CM000669.2:g.128857253T>C GRCh38
NC_000007.13:g.128497307T>C , CM000669.1:g.128497307T>C GRCh37
NC_000007.12:g.128284543T>C NCBI36
NG_011807.1:g.31825T>C , LRG_870:g.31825T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7697T>C (FLNC) MANE Select ENSP00000327145.8:p.Met2566Thr
ENST00000325888.12:c.7697T>C (FLNC) ENSP00000327145.8:p.Met2566Thr
ENST00000346177.6:c.7598T>C (FLNC) ENSP00000344002.6:p.Met2533Thr
NM_001127487.1:c.7598T>C (FLNC) NP_001120959.1:p.Met2533Thr
NM_001458.4:c.7697T>C , LRG_870t1:c.7697T>C (FLNC) NP_001449.3:p.Met2566Thr
NR_149055.1:n.103-3856A>G (FLNC-AS1)
NM_001127487.2:c.7598T>C (FLNC) NP_001120959.1:p.Met2533Thr
NM_001458.5:c.7697T>C (FLNC) MANE Select NP_001449.3:p.Met2566Thr
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Search 100 bp 3'