Canonical Allele Identifier: CA166190309
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs766936904

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853018C>A , CM000669.2:g.128853018C>A GRCh38
NC_000007.13:g.128493072C>A , CM000669.1:g.128493072C>A GRCh37
NC_000007.12:g.128280308C>A NCBI36
NG_011807.1:g.27590C>A , LRG_870:g.27590C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6195C>A (FLNC) MANE Select ENSP00000327145.8:p.Asp2065Glu
ENST00000325888.12:c.6195C>A (FLNC) ENSP00000327145.8:p.Asp2065Glu
ENST00000346177.6:c.6096C>A (FLNC) ENSP00000344002.6:p.Asp2032Glu
NM_001127487.1:c.6096C>A (FLNC) NP_001120959.1:p.Asp2032Glu
NM_001458.4:c.6195C>A , LRG_870t1:c.6195C>A (FLNC) NP_001449.3:p.Asp2065Glu
NR_149055.1:n.215+267G>T (FLNC-AS1)
NM_001127487.2:c.6096C>A (FLNC) NP_001120959.1:p.Asp2032Glu
NM_001458.5:c.6195C>A (FLNC) MANE Select NP_001449.3:p.Asp2065Glu