Canonical Allele Identifier: CA4476445
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs767890706
ExAC: 7:128498610 A / C
gnomAD v2: 7-128498610-A-C
gnomAD v3: 7-128858556-A-C
gnomAD v4: 7-128858556-A-C
MyVariant Identifiers: chr7:g.128498610A>C (hg19) chr7:g.128858556A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858556A>C , CM000669.2:g.128858556A>C GRCh38
NC_000007.13:g.128498610A>C , CM000669.1:g.128498610A>C GRCh37
NC_000007.12:g.128285846A>C NCBI36
NG_011807.1:g.33128A>C , LRG_870:g.33128A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*33A>C (FLNC) MANE Select ENSP00000327145.8:n.*33A>C
ENST00000325888.12:c.*33A>C (FLNC) ENSP00000327145.8:n.*33A>C
ENST00000346177.6:c.*33A>C (FLNC) ENSP00000344002.6:n.*33A>C
NM_001127487.1:c.*33A>C (FLNC) NP_001120959.1:n.*33A>C
NM_001458.4:c.*33A>C , LRG_870t1:c.*33A>C (FLNC) NP_001449.3:n.*33A>C
NR_149055.1:n.102+3969T>G (FLNC-AS1)
NM_001127487.2:c.*33A>C (FLNC) NP_001120959.1:n.*33A>C
NM_001458.5:c.*33A>C (FLNC) MANE Select NP_001449.3:n.*33A>C
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