Canonical Allele Identifier: CA369219717
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1421296226

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857253T>A , CM000669.2:g.128857253T>A GRCh38
NC_000007.13:g.128497307T>A , CM000669.1:g.128497307T>A GRCh37
NC_000007.12:g.128284543T>A NCBI36
NG_011807.1:g.31825T>A , LRG_870:g.31825T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7697T>A (FLNC) MANE Select ENSP00000327145.8:p.Met2566Lys
ENST00000325888.12:c.7697T>A (FLNC) ENSP00000327145.8:p.Met2566Lys
ENST00000346177.6:c.7598T>A (FLNC) ENSP00000344002.6:p.Met2533Lys
NM_001127487.1:c.7598T>A (FLNC) NP_001120959.1:p.Met2533Lys
NM_001458.4:c.7697T>A , LRG_870t1:c.7697T>A (FLNC) NP_001449.3:p.Met2566Lys
NR_149055.1:n.103-3856A>T (FLNC-AS1)
NM_001127487.2:c.7598T>A (FLNC) NP_001120959.1:p.Met2533Lys
NM_001458.5:c.7697T>A (FLNC) MANE Select NP_001449.3:p.Met2566Lys