Canonical Allele Identifier: CA457850778

Gene: FLNC FLNC-AS1

Linked Data

• MyVariant Identifiers: chr7:g.128497372del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857319del , CM000669.2:g.128857319del	GRCh38
NC_000007.13:g.128497373del , CM000669.1:g.128497373del	GRCh37
NC_000007.12:g.128284609del	NCBI36
NG_011807.1:g.31891del , LRG_870:g.31891del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7763del (FLNC) MANE Select	ENSP00000327145.8:p.Phe2588SerfsTer27
ENST00000325888.12:c.7763del (FLNC)	ENSP00000327145.8:p.Phe2588SerfsTer27
ENST00000346177.6:c.7664del (FLNC)	ENSP00000344002.6:p.Phe2555SerfsTer27
NM_001127487.1:c.7664del (FLNC)	NP_001120959.1:p.Phe2555SerfsTer27
NM_001458.4:c.7763del , LRG_870t1:c.7763del (FLNC)	NP_001449.3:p.Phe2588SerfsTer27
NR_149055.1:n.103-3921del (FLNC-AS1)
NM_001127487.2:c.7664del (FLNC)	NP_001120959.1:p.Phe2555SerfsTer27
NM_001458.5:c.7763del (FLNC) MANE Select	NP_001449.3:p.Phe2588SerfsTer27