Canonical Allele Identifier: CA578151188

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1563006313
• gnomAD v2: 7-128498674-G-GCACA
• gnomAD v3: 7-128858620-G-GCACA
• gnomAD v4: 7-128858620-G-GCACA
• MyVariant Identifiers: chr7:g.128498674_128498675insCACA (hg19) ; chr7:g.128858620_128858621insCACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858621_128858624dup , CM000669.2:g.128858621_128858624dup	GRCh38
NC_000007.13:g.128498675_128498678dup , CM000669.1:g.128498675_128498678dup	GRCh37
NC_000007.12:g.128285911_128285914dup	NCBI36
NG_011807.1:g.33193_33196dup , LRG_870:g.33193_33196dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.*98_*101dup (FLNC) MANE Select	ENSP00000327145.8:n.*98_*101dup
ENST00000325888.12:c.*98_*101dup (FLNC)	ENSP00000327145.8:n.*98_*101dup
ENST00000346177.6:c.*98_*101dup (FLNC)	ENSP00000344002.6:n.*98_*101dup
NM_001127487.1:c.*98_*101dup (FLNC)	NP_001120959.1:n.*98_*101dup
NM_001458.4:c.*98_*101dup , LRG_870t1:c.*98_*101dup (FLNC)	NP_001449.3:n.*98_*101dup
NR_149055.1:n.102+3901_102+3904dup (FLNC-AS1)
NM_001127487.2:c.*98_*101dup (FLNC)	NP_001120959.1:n.*98_*101dup
NM_001458.5:c.*98_*101dup (FLNC) MANE Select	NP_001449.3:n.*98_*101dup