Canonical Allele Identifier: CA4476441
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs763569510
ExAC: 7:128498588 T / C
gnomAD v2: 7-128498588-T-C
gnomAD v3: 7-128858534-T-C
gnomAD v4: 7-128858534-T-C
MyVariant Identifiers: chr7:g.128498588T>C (hg19) chr7:g.128858534T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858534T>C , CM000669.2:g.128858534T>C GRCh38
NC_000007.13:g.128498588T>C , CM000669.1:g.128498588T>C GRCh37
NC_000007.12:g.128285824T>C NCBI36
NG_011807.1:g.33106T>C , LRG_870:g.33106T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*11T>C (FLNC) MANE Select ENSP00000327145.8:n.*11T>C
ENST00000325888.12:c.*11T>C (FLNC) ENSP00000327145.8:n.*11T>C
ENST00000346177.6:c.*11T>C (FLNC) ENSP00000344002.6:n.*11T>C
NM_001127487.1:c.*11T>C (FLNC) NP_001120959.1:n.*11T>C
NM_001458.4:c.*11T>C , LRG_870t1:c.*11T>C (FLNC) NP_001449.3:n.*11T>C
NR_149055.1:n.102+3991A>G (FLNC-AS1)
NM_001127487.2:c.*11T>C (FLNC) NP_001120959.1:n.*11T>C
NM_001458.5:c.*11T>C (FLNC) MANE Select NP_001449.3:n.*11T>C
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Search 100 bp 3'