Canonical Allele Identifier: CA369191668
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2264304
ClinVar RCV Id: RCV002803280
gnomAD v4: 7-128842865-A-G
MyVariant Identifiers: chr7:g.128482919A>G (hg19) chr7:g.128842865A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842865A>G , CM000669.2:g.128842865A>G GRCh38
NC_000007.13:g.128482919A>G , CM000669.1:g.128482919A>G GRCh37
NC_000007.12:g.128270155A>G NCBI36
NG_011807.1:g.17437A>G , LRG_870:g.17437A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2461A>G MANE Select ENSP00000327145.8:p.Ile821Val
ENST00000325888.12:c.2461A>G ENSP00000327145.8:p.Ile821Val
ENST00000346177.6:c.2461A>G ENSP00000344002.6:p.Ile821Val
NM_001127487.1:c.2461A>G NP_001120959.1:p.Ile821Val
NM_001458.4:c.2461A>G , LRG_870t1:c.2461A>G NP_001449.3:p.Ile821Val
NM_001127487.2:c.2461A>G NP_001120959.1:p.Ile821Val
NM_001458.5:c.2461A>G MANE Select NP_001449.3:p.Ile821Val
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