Canonical Allele Identifier: CA4475068
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1215085
ClinVar RCV Id: RCV001593560 RCV002072322 RCV002458547
dbSNP Id: rs774467047
ExAC: 7:128485077 G / A
gnomAD v2: 7-128485077-G-A
gnomAD v3: 7-128845023-G-A
gnomAD v4: 7-128845023-G-A
COSMIC: COSM1085362
MyVariant Identifiers: chr7:g.128485077G>A (hg19) chr7:g.128845023G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128845023G>A , CM000669.2:g.128845023G>A GRCh38
NC_000007.13:g.128485077G>A , CM000669.1:g.128485077G>A GRCh37
NC_000007.12:g.128272313G>A NCBI36
NG_011807.1:g.19595G>A , LRG_870:g.19595G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.3558G>A MANE Select ENSP00000327145.8:p.Ala1186=
ENST00000325888.12:c.3558G>A ENSP00000327145.8:p.Ala1186=
ENST00000346177.6:c.3558G>A ENSP00000344002.6:p.Ala1186=
NM_001127487.1:c.3558G>A NP_001120959.1:p.Ala1186=
NM_001458.4:c.3558G>A , LRG_870t1:c.3558G>A NP_001449.3:p.Ala1186=
NM_001127487.2:c.3558G>A NP_001120959.1:p.Ala1186=
NM_001458.5:c.3558G>A MANE Select NP_001449.3:p.Ala1186=
Search 100 bp 5'
Search 100 bp 3'