Canonical Allele Identifier: CA1742550584

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857371_128857376delinsGCAGCC , CM000669.2:g.128857371_128857376delinsGCAGCC	GRCh38
NC_000007.13:g.128497425_128497430delinsGCAGCC , CM000669.1:g.128497425_128497430delinsGCAGCC	GRCh37
NC_000007.12:g.128284661_128284666delinsGCAGCC	NCBI36
NG_011807.1:g.31943_31948delinsGCAGCC , LRG_870:g.31943_31948delinsGCAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+35_7780+40delinsGCAGCC (FLNC) MANE Select	ENSP00000327145.8:n.7780+35_7780+40delinsGCAGCC
ENST00000325888.12:c.7780+35_7780+40delinsGCAGCC (FLNC)	ENSP00000327145.8:n.7780+35_7780+40delinsGCAGCC
ENST00000346177.6:c.7681+35_7681+40delinsGCAGCC (FLNC)	ENSP00000344002.6:n.7681+35_7681+40delinsGCAGCC
NM_001127487.1:c.7681+35_7681+40delinsGCAGCC (FLNC)	NP_001120959.1:n.7681+35_7681+40delinsGCAGCC
NM_001458.4:c.7780+35_7780+40delinsGCAGCC , LRG_870t1:c.7780+35_7780+40delinsGCAGCC (FLNC)	NP_001449.3:n.7780+35_7780+40delinsGCAGCC
NR_149055.1:n.103-3979_103-3974delinsGGCTGC (FLNC-AS1)
NM_001127487.2:c.7681+35_7681+40delinsGCAGCC (FLNC)	NP_001120959.1:n.7681+35_7681+40delinsGCAGCC
NM_001458.5:c.7780+35_7780+40delinsGCAGCC (FLNC) MANE Select	NP_001449.3:n.7780+35_7780+40delinsGCAGCC