Canonical Allele Identifier: CA369220083
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128498101C>T (hg19) chr7:g.128858047C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858047C>T , CM000669.2:g.128858047C>T GRCh38
NC_000007.13:g.128498101C>T , CM000669.1:g.128498101C>T GRCh37
NC_000007.12:g.128285337C>T NCBI36
NG_011807.1:g.32619C>T , LRG_870:g.32619C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7820C>T (FLNC) MANE Select ENSP00000327145.8:p.Ser2607Phe
ENST00000325888.12:c.7820C>T (FLNC) ENSP00000327145.8:p.Ser2607Phe
ENST00000346177.6:c.7721C>T (FLNC) ENSP00000344002.6:p.Ser2574Phe
NM_001127487.1:c.7721C>T (FLNC) NP_001120959.1:p.Ser2574Phe
NM_001458.4:c.7820C>T , LRG_870t1:c.7820C>T (FLNC) NP_001449.3:p.Ser2607Phe
NR_149055.1:n.102+4478G>A (FLNC-AS1)
NM_001127487.2:c.7721C>T (FLNC) NP_001120959.1:p.Ser2574Phe
NM_001458.5:c.7820C>T (FLNC) MANE Select NP_001449.3:p.Ser2607Phe
Search 100 bp 5'
Search 100 bp 3'