Canonical Allele Identifier: CA2580611033
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2945653
ClinVar RCV Id: RCV003803747

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852832del , CM000669.2:g.128852832del GRCh38
NC_000007.13:g.128492886del , CM000669.1:g.128492886del GRCh37
NC_000007.12:g.128280122del NCBI36
NG_011807.1:g.27404del , LRG_870:g.27404del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6009del (FLNC) MANE Select ENSP00000327145.8:p.Ser2004ProfsTer12
ENST00000325888.12:c.6009del (FLNC) ENSP00000327145.8:p.Ser2004ProfsTer12
ENST00000346177.6:c.5910del (FLNC) ENSP00000344002.6:p.Ser1971ProfsTer12
NM_001127487.1:c.5910del (FLNC) NP_001120959.1:p.Ser1971ProfsTer12
NM_001458.4:c.6009del , LRG_870t1:c.6009del (FLNC) NP_001449.3:p.Ser2004ProfsTer12
NR_149055.1:n.215+453del (FLNC-AS1)
NM_001127487.2:c.5910del (FLNC) NP_001120959.1:p.Ser1971ProfsTer12
NM_001458.5:c.6009del (FLNC) MANE Select NP_001449.3:p.Ser2004ProfsTer12