Canonical Allele Identifier: CA1742551901

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858236_128858237delinsGC , CM000669.2:g.128858236_128858237delinsGC	GRCh38
NC_000007.13:g.128498290_128498291delinsGC , CM000669.1:g.128498290_128498291delinsGC	GRCh37
NC_000007.12:g.128285526_128285527delinsGC	NCBI36
NG_011807.1:g.32808_32809delinsGC , LRG_870:g.32808_32809delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7990+19_7990+20delinsGC (FLNC) MANE Select	ENSP00000327145.8:n.7990+19_7990+20delinsGC
ENST00000325888.12:c.7990+19_7990+20delinsGC (FLNC)	ENSP00000327145.8:n.7990+19_7990+20delinsGC
ENST00000346177.6:c.7891+19_7891+20delinsGC (FLNC)	ENSP00000344002.6:n.7891+19_7891+20delinsGC
NM_001127487.1:c.7891+19_7891+20delinsGC (FLNC)	NP_001120959.1:n.7891+19_7891+20delinsGC
NM_001458.4:c.7990+19_7990+20delinsGC , LRG_870t1:c.7990+19_7990+20delinsGC (FLNC)	NP_001449.3:n.7990+19_7990+20delinsGC
NR_149055.1:n.102+4288_102+4289delinsGC (FLNC-AS1)
NM_001127487.2:c.7891+19_7891+20delinsGC (FLNC)	NP_001120959.1:n.7891+19_7891+20delinsGC
NM_001458.5:c.7990+19_7990+20delinsGC (FLNC) MANE Select	NP_001449.3:n.7990+19_7990+20delinsGC