Canonical Allele Identifier: CA166196778
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs28609612
gnomAD v2: 7-128498674-G-A
gnomAD v3: 7-128858620-G-A
gnomAD v4: 7-128858620-G-A
MyVariant Identifiers: chr7:g.128498674G>A (hg19) chr7:g.128858620G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858620G>A , CM000669.2:g.128858620G>A GRCh38
NC_000007.13:g.128498674G>A , CM000669.1:g.128498674G>A GRCh37
NC_000007.12:g.128285910G>A NCBI36
NG_011807.1:g.33192G>A , LRG_870:g.33192G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*97G>A (FLNC) MANE Select ENSP00000327145.8:n.*97G>A
ENST00000325888.12:c.*97G>A (FLNC) ENSP00000327145.8:n.*97G>A
ENST00000346177.6:c.*97G>A (FLNC) ENSP00000344002.6:n.*97G>A
NM_001127487.1:c.*97G>A (FLNC) NP_001120959.1:n.*97G>A
NM_001458.4:c.*97G>A , LRG_870t1:c.*97G>A (FLNC) NP_001449.3:n.*97G>A
NR_149055.1:n.102+3905C>T (FLNC-AS1)
NM_001127487.2:c.*97G>A (FLNC) NP_001120959.1:n.*97G>A
NM_001458.5:c.*97G>A (FLNC) MANE Select NP_001449.3:n.*97G>A
Search 100 bp 5'
Search 100 bp 3'