Canonical Allele Identifier: CA4475343
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1192821
ClinVar RCV Id: RCV001555008
dbSNP Id: rs199606672
ExAC: 7:128487961 C / T
gnomAD v2: 7-128487961-C-T
gnomAD v3: 7-128847907-C-T
gnomAD v4: 7-128847907-C-T
MyVariant Identifiers: chr7:g.128487961C>T (hg19) chr7:g.128847907C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847907C>T , CM000669.2:g.128847907C>T GRCh38
NC_000007.13:g.128487961C>T , CM000669.1:g.128487961C>T GRCh37
NC_000007.12:g.128275197C>T NCBI36
NG_011807.1:g.22479C>T , LRG_870:g.22479C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4457-38C>T MANE Select ENSP00000327145.8:n.4457-38C>T
ENST00000325888.12:c.4457-38C>T ENSP00000327145.8:n.4457-38C>T
ENST00000346177.6:c.4457-38C>T ENSP00000344002.6:n.4457-38C>T
NM_001127487.1:c.4457-38C>T NP_001120959.1:n.4457-38C>T
NM_001458.4:c.4457-38C>T , LRG_870t1:c.4457-38C>T NP_001449.3:n.4457-38C>T
NM_001127487.2:c.4457-38C>T NP_001120959.1:n.4457-38C>T
NM_001458.5:c.4457-38C>T MANE Select NP_001449.3:n.4457-38C>T
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