Canonical Allele Identifier: CA658657723
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 472109
ClinVar RCV Id: RCV001508595 RCV002358571 RCV003486880
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851549_128851550delinsCA , CM000669.2:g.128851549_128851550delinsCA GRCh38
NC_000007.13:g.128491603_128491604delinsCA , CM000669.1:g.128491603_128491604delinsCA GRCh37
NC_000007.12:g.128278839_128278840delinsCA NCBI36
NG_011807.1:g.26121_26122delinsCA , LRG_870:g.26121_26122delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5763_5764delinsCA (FLNC) MANE Select ENSP00000327145.8:p.Ala1922Thr
ENST00000325888.12:c.5763_5764delinsCA (FLNC) ENSP00000327145.8:p.Ala1922Thr
ENST00000346177.6:c.5664_5665delinsCA (FLNC) ENSP00000344002.6:p.Ala1889Thr
NM_001127487.1:c.5664_5665delinsCA (FLNC) NP_001120959.1:p.Ala1889Thr
NM_001458.4:c.5763_5764delinsCA , LRG_870t1:c.5763_5764delinsCA (FLNC) NP_001449.3:p.Ala1922Thr
NR_149055.1:n.216-50_216-49delinsTG (FLNC-AS1)
NM_001127487.2:c.5664_5665delinsCA (FLNC) NP_001120959.1:p.Ala1889Thr
NM_001458.5:c.5763_5764delinsCA (FLNC) MANE Select NP_001449.3:p.Ala1922Thr
Search 100 bp 5'
Search 100 bp 3'