Canonical Allele Identifier: CA2579014538

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128851672_128851673dup , CM000669.2:g.128851672_128851673dup	GRCh38
NC_000007.13:g.128491726_128491727dup , CM000669.1:g.128491726_128491727dup	GRCh37
NC_000007.12:g.128278962_128278963dup	NCBI36
NG_011807.1:g.26244_26245dup , LRG_870:g.26244_26245dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.5842+44_5842+45dup (FLNC) MANE Select	ENSP00000327145.8:n.5842+44_5842+45dup
ENST00000325888.12:c.5842+44_5842+45dup (FLNC)	ENSP00000327145.8:n.5842+44_5842+45dup
ENST00000346177.6:c.5743+44_5743+45dup (FLNC)	ENSP00000344002.6:n.5743+44_5743+45dup
NM_001127487.1:c.5743+44_5743+45dup (FLNC)	NP_001120959.1:n.5743+44_5743+45dup
NM_001458.4:c.5842+44_5842+45dup , LRG_870t1:c.5842+44_5842+45dup (FLNC)	NP_001449.3:n.5842+44_5842+45dup
NR_149055.1:n.216-166_216-165dup (FLNC-AS1)
NM_001127487.2:c.5743+44_5743+45dup (FLNC)	NP_001120959.1:n.5743+44_5743+45dup
NM_001458.5:c.5842+44_5842+45dup (FLNC) MANE Select	NP_001449.3:n.5842+44_5842+45dup