Canonical Allele Identifier: CA4475012
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 425426
ClinVar RCV Id: RCV000487754 RCV002323848 RCV001368325 RCV003150239
dbSNP Id: rs759452636
ExAC: 7:128484814 G / A
gnomAD v2: 7-128484814-G-A
gnomAD v3: 7-128844760-G-A
gnomAD v4: 7-128844760-G-A
MyVariant Identifiers: chr7:g.128484814G>A (hg19) chr7:g.128844760G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128844760G>A , CM000669.2:g.128844760G>A GRCh38
NC_000007.13:g.128484814G>A , CM000669.1:g.128484814G>A GRCh37
NC_000007.12:g.128272050G>A NCBI36
NG_011807.1:g.19332G>A , LRG_870:g.19332G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3295G>A MANE Select ENSP00000327145.8:p.Val1099Ile
ENST00000325888.12:c.3295G>A ENSP00000327145.8:p.Val1099Ile
ENST00000346177.6:c.3295G>A ENSP00000344002.6:p.Val1099Ile
NM_001127487.1:c.3295G>A NP_001120959.1:p.Val1099Ile
NM_001458.4:c.3295G>A , LRG_870t1:c.3295G>A NP_001449.3:p.Val1099Ile
NM_001127487.2:c.3295G>A NP_001120959.1:p.Val1099Ile
NM_001458.5:c.3295G>A MANE Select NP_001449.3:p.Val1099Ile
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