Canonical Allele Identifier: CA2684820808
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858653G>T , CM000669.2:g.128858653G>T GRCh38
NC_000007.13:g.128498707G>T , CM000669.1:g.128498707G>T GRCh37
NC_000007.12:g.128285943G>T NCBI36
NG_011807.1:g.33225G>T , LRG_870:g.33225G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*130G>T (FLNC) MANE Select ENSP00000327145.8:n.*130G>T
ENST00000325888.12:c.*130G>T (FLNC) ENSP00000327145.8:n.*130G>T
ENST00000346177.6:c.*130G>T (FLNC) ENSP00000344002.6:n.*130G>T
NM_001127487.1:c.*130G>T (FLNC) NP_001120959.1:n.*130G>T
NM_001458.4:c.*130G>T , LRG_870t1:c.*130G>T (FLNC) NP_001449.3:n.*130G>T
NR_149055.1:n.102+3872C>A (FLNC-AS1)
NM_001127487.2:c.*130G>T (FLNC) NP_001120959.1:n.*130G>T
NM_001458.5:c.*130G>T (FLNC) MANE Select NP_001449.3:n.*130G>T