Canonical Allele Identifier: CA1107056585
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1809172497

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858577_128858578insTACA , CM000669.2:g.128858577_128858578insTACA GRCh38
NC_000007.13:g.128498631_128498632insTACA , CM000669.1:g.128498631_128498632insTACA GRCh37
NC_000007.12:g.128285867_128285868insTACA NCBI36
NG_011807.1:g.33149_33150insTACA , LRG_870:g.33149_33150insTACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*54_*55insTACA (FLNC) MANE Select ENSP00000327145.8:n.*54_*55insTACA
ENST00000325888.12:c.*54_*55insTACA (FLNC) ENSP00000327145.8:n.*54_*55insTACA
ENST00000346177.6:c.*54_*55insTACA (FLNC) ENSP00000344002.6:n.*54_*55insTACA
NM_001127487.1:c.*54_*55insTACA (FLNC) NP_001120959.1:n.*54_*55insTACA
NM_001458.4:c.*54_*55insTACA , LRG_870t1:c.*54_*55insTACA (FLNC) NP_001449.3:n.*54_*55insTACA
NR_149055.1:n.102+3948_102+3949insGTAT (FLNC-AS1)
NM_001127487.2:c.*54_*55insTACA (FLNC) NP_001120959.1:n.*54_*55insTACA
NM_001458.5:c.*54_*55insTACA (FLNC) MANE Select NP_001449.3:n.*54_*55insTACA