Canonical Allele Identifier: CA1107056614
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1809175258

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858609C>T , CM000669.2:g.128858609C>T GRCh38
NC_000007.13:g.128498663C>T , CM000669.1:g.128498663C>T GRCh37
NC_000007.12:g.128285899C>T NCBI36
NG_011807.1:g.33181C>T , LRG_870:g.33181C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*86C>T (FLNC) MANE Select ENSP00000327145.8:n.*86C>T
ENST00000325888.12:c.*86C>T (FLNC) ENSP00000327145.8:n.*86C>T
ENST00000346177.6:c.*86C>T (FLNC) ENSP00000344002.6:n.*86C>T
NM_001127487.1:c.*86C>T (FLNC) NP_001120959.1:n.*86C>T
NM_001458.4:c.*86C>T , LRG_870t1:c.*86C>T (FLNC) NP_001449.3:n.*86C>T
NR_149055.1:n.102+3916G>A (FLNC-AS1)
NM_001127487.2:c.*86C>T (FLNC) NP_001120959.1:n.*86C>T
NM_001458.5:c.*86C>T (FLNC) MANE Select NP_001449.3:n.*86C>T