Canonical Allele Identifier: CA2684813855
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853185_128853186insTTCACTTTCCCGC , CM000669.2:g.128853185_128853186insTTCACTTTCCCGC GRCh38
NC_000007.13:g.128493239_128493240insTTCACTTTCCCGC , CM000669.1:g.128493239_128493240insTTCACTTTCCCGC GRCh37
NC_000007.12:g.128280475_128280476insTTCACTTTCCCGC NCBI36
NG_011807.1:g.27757_27758insTTCACTTTCCCGC , LRG_870:g.27757_27758insTTCACTTTCCCGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6208+154_6208+155insTTCACTTTCCCGC (FLNC) MANE Select ENSP00000327145.8:n.6208+154_6208+155insTTCACTTTCCCGC
ENST00000325888.12:c.6208+154_6208+155insTTCACTTTCCCGC (FLNC) ENSP00000327145.8:n.6208+154_6208+155insTTCACTTTCCCGC
ENST00000346177.6:c.6109+154_6109+155insTTCACTTTCCCGC (FLNC) ENSP00000344002.6:n.6109+154_6109+155insTTCACTTTCCCGC
NM_001127487.1:c.6109+154_6109+155insTTCACTTTCCCGC (FLNC) NP_001120959.1:n.6109+154_6109+155insTTCACTTTCCCGC
NM_001458.4:c.6208+154_6208+155insTTCACTTTCCCGC , LRG_870t1:c.6208+154_6208+155insTTCACTTTCCCGC (FLNC) NP_001449.3:n.6208+154_6208+155insTTCACTTTCCCGC
NR_149055.1:n.215+99_215+100insGCGGGAAAGTGAA (FLNC-AS1)
NM_001127487.2:c.6109+154_6109+155insTTCACTTTCCCGC (FLNC) NP_001120959.1:n.6109+154_6109+155insTTCACTTTCCCGC
NM_001458.5:c.6208+154_6208+155insTTCACTTTCCCGC (FLNC) MANE Select NP_001449.3:n.6208+154_6208+155insTTCACTTTCCCGC