Canonical Allele Identifier: CA2684814861

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128853814-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853815del , CM000669.2:g.128853815del	GRCh38
NC_000007.13:g.128493869del , CM000669.1:g.128493869del	GRCh37
NC_000007.12:g.128281105del	NCBI36
NG_011807.1:g.28387del , LRG_870:g.28387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6462del (FLNC) MANE Select	ENSP00000327145.8:p.Cys2154TrpfsTer21
ENST00000325888.12:c.6462del (FLNC)	ENSP00000327145.8:p.Cys2154TrpfsTer21
ENST00000346177.6:c.6363del (FLNC)	ENSP00000344002.6:p.Cys2121TrpfsTer21
NM_001127487.1:c.6363del (FLNC)	NP_001120959.1:p.Cys2121TrpfsTer21
NM_001458.4:c.6462del , LRG_870t1:c.6462del (FLNC)	NP_001449.3:p.Cys2154TrpfsTer21
NR_149055.1:n.103-418del (FLNC-AS1)
NM_001127487.2:c.6363del (FLNC)	NP_001120959.1:p.Cys2121TrpfsTer21
NM_001458.5:c.6462del (FLNC) MANE Select	NP_001449.3:p.Cys2154TrpfsTer21