Canonical Allele Identifier: CA4476355

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs751456369
• ExAC: 7:128497425 G / GCAGCC
• gnomAD v4: 7-128857371-G-GCAGCC
• MyVariant Identifiers: chr7:g.128497430_128497431insCAGCC (hg19) ; chr7:g.128497425_128497426insCAGCC (hg19) ; chr7:g.128857371_128857372insCAGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857382_128857386dup , CM000669.2:g.128857382_128857386dup	GRCh38
NC_000007.13:g.128497436_128497440dup , CM000669.1:g.128497436_128497440dup	GRCh37
NC_000007.12:g.128284672_128284676dup	NCBI36
NG_011807.1:g.31954_31958dup , LRG_870:g.31954_31958dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+46_7780+50dup (FLNC) MANE Select	ENSP00000327145.8:n.7780+46_7780+50dup
ENST00000325888.12:c.7780+46_7780+50dup (FLNC)	ENSP00000327145.8:n.7780+46_7780+50dup
ENST00000346177.6:c.7681+46_7681+50dup (FLNC)	ENSP00000344002.6:n.7681+46_7681+50dup
NM_001127487.1:c.7681+46_7681+50dup (FLNC)	NP_001120959.1:n.7681+46_7681+50dup
NM_001458.4:c.7780+46_7780+50dup , LRG_870t1:c.7780+46_7780+50dup (FLNC)	NP_001449.3:n.7780+46_7780+50dup
NR_149055.1:n.103-3979_103-3975dup (FLNC-AS1)
NM_001127487.2:c.7681+46_7681+50dup (FLNC)	NP_001120959.1:n.7681+46_7681+50dup
NM_001458.5:c.7780+46_7780+50dup (FLNC) MANE Select	NP_001449.3:n.7780+46_7780+50dup