Canonical Allele Identifier: CA457849536
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128852973-G-A
MyVariant Identifiers: chr7:g.128493027G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852973G>A , CM000669.2:g.128852973G>A GRCh38
NC_000007.13:g.128493027G>A , CM000669.1:g.128493027G>A GRCh37
NC_000007.12:g.128280263G>A NCBI36
NG_011807.1:g.27545G>A , LRG_870:g.27545G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6150G>A (FLNC) MANE Select ENSP00000327145.8:p.Gly2050=
ENST00000325888.12:c.6150G>A (FLNC) ENSP00000327145.8:p.Gly2050=
ENST00000346177.6:c.6051G>A (FLNC) ENSP00000344002.6:p.Gly2017=
NM_001127487.1:c.6051G>A (FLNC) NP_001120959.1:p.Gly2017=
NM_001458.4:c.6150G>A , LRG_870t1:c.6150G>A (FLNC) NP_001449.3:p.Gly2050=
NR_149055.1:n.215+312C>T (FLNC-AS1)
NM_001127487.2:c.6051G>A (FLNC) NP_001120959.1:p.Gly2017=
NM_001458.5:c.6150G>A (FLNC) MANE Select NP_001449.3:p.Gly2050=
Search 100 bp 5'
Search 100 bp 3'