Canonical Allele Identifier: CA369208080
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128491545C>G (hg19) chr7:g.128851491C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851491C>G , CM000669.2:g.128851491C>G GRCh38
NC_000007.13:g.128491545C>G , CM000669.1:g.128491545C>G GRCh37
NC_000007.12:g.128278781C>G NCBI36
NG_011807.1:g.26063C>G , LRG_870:g.26063C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5705C>G (FLNC) MANE Select ENSP00000327145.8:p.Ala1902Gly
ENST00000325888.12:c.5705C>G (FLNC) ENSP00000327145.8:p.Ala1902Gly
ENST00000346177.6:c.5606C>G (FLNC) ENSP00000344002.6:p.Ala1869Gly
NM_001127487.1:c.5606C>G (FLNC) NP_001120959.1:p.Ala1869Gly
NM_001458.4:c.5705C>G , LRG_870t1:c.5705C>G (FLNC) NP_001449.3:p.Ala1902Gly
NR_149055.1:n.225G>C (FLNC-AS1)
NM_001127487.2:c.5606C>G (FLNC) NP_001120959.1:p.Ala1869Gly
NM_001458.5:c.5705C>G (FLNC) MANE Select NP_001449.3:p.Ala1902Gly
Search 100 bp 5'
Search 100 bp 3'