Canonical Allele Identifier: CA369191684
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1205831
ClinVar RCV Id: RCV001572612
dbSNP Id: rs2128935776
MyVariant Identifiers: chr7:g.128482926A>G (hg19) chr7:g.128842872A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842872A>G , CM000669.2:g.128842872A>G GRCh38
NC_000007.13:g.128482926A>G , CM000669.1:g.128482926A>G GRCh37
NC_000007.12:g.128270162A>G NCBI36
NG_011807.1:g.17444A>G , LRG_870:g.17444A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2468A>G MANE Select ENSP00000327145.8:p.Lys823Arg
ENST00000325888.12:c.2468A>G ENSP00000327145.8:p.Lys823Arg
ENST00000346177.6:c.2468A>G ENSP00000344002.6:p.Lys823Arg
NM_001127487.1:c.2468A>G NP_001120959.1:p.Lys823Arg
NM_001458.4:c.2468A>G , LRG_870t1:c.2468A>G NP_001449.3:p.Lys823Arg
NM_001127487.2:c.2468A>G NP_001120959.1:p.Lys823Arg
NM_001458.5:c.2468A>G MANE Select NP_001449.3:p.Lys823Arg
Search 100 bp 5'
Search 100 bp 3'