Canonical Allele Identifier: CA369211705
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128493083C>A (hg19) chr7:g.128853029C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853029C>A , CM000669.2:g.128853029C>A GRCh38
NC_000007.13:g.128493083C>A , CM000669.1:g.128493083C>A GRCh37
NC_000007.12:g.128280319C>A NCBI36
NG_011807.1:g.27601C>A , LRG_870:g.27601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6206C>A (FLNC) MANE Select ENSP00000327145.8:p.Ala2069Glu
ENST00000325888.12:c.6206C>A (FLNC) ENSP00000327145.8:p.Ala2069Glu
ENST00000346177.6:c.6107C>A (FLNC) ENSP00000344002.6:p.Ala2036Glu
NM_001127487.1:c.6107C>A (FLNC) NP_001120959.1:p.Ala2036Glu
NM_001458.4:c.6206C>A , LRG_870t1:c.6206C>A (FLNC) NP_001449.3:p.Ala2069Glu
NR_149055.1:n.215+256G>T (FLNC-AS1)
NM_001127487.2:c.6107C>A (FLNC) NP_001120959.1:p.Ala2036Glu
NM_001458.5:c.6206C>A (FLNC) MANE Select NP_001449.3:p.Ala2069Glu
Search 100 bp 5'
Search 100 bp 3'