Canonical Allele Identifier: CA2777853546

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858247_128858248dup , CM000669.2:g.128858247_128858248dup	GRCh38
NC_000007.13:g.128498301_128498302dup , CM000669.1:g.128498301_128498302dup	GRCh37
NC_000007.12:g.128285537_128285538dup	NCBI36
NG_011807.1:g.32819_32820dup , LRG_870:g.32819_32820dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7990+30_7990+31dup (FLNC) MANE Select	ENSP00000327145.8:n.7990+30_7990+31dup
ENST00000325888.12:c.7990+30_7990+31dup (FLNC)	ENSP00000327145.8:n.7990+30_7990+31dup
ENST00000346177.6:c.7891+30_7891+31dup (FLNC)	ENSP00000344002.6:n.7891+30_7891+31dup
NM_001127487.1:c.7891+30_7891+31dup (FLNC)	NP_001120959.1:n.7891+30_7891+31dup
NM_001458.4:c.7990+30_7990+31dup , LRG_870t1:c.7990+30_7990+31dup (FLNC)	NP_001449.3:n.7990+30_7990+31dup
NR_149055.1:n.102+4279_102+4280dup (FLNC-AS1)
NM_001127487.2:c.7891+30_7891+31dup (FLNC)	NP_001120959.1:n.7891+30_7891+31dup
NM_001458.5:c.7990+30_7990+31dup (FLNC) MANE Select	NP_001449.3:n.7990+30_7990+31dup