Canonical Allele Identifier: CA1742575325

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128852785_128852786delinsTG , CM000669.2:g.128852785_128852786delinsTG	GRCh38
NC_000007.13:g.128492839_128492840delinsTG , CM000669.1:g.128492839_128492840delinsTG	GRCh37
NC_000007.12:g.128280075_128280076delinsTG	NCBI36
NG_011807.1:g.27357_27358delinsTG , LRG_870:g.27357_27358delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6004+33_6004+34delinsTG (FLNC) MANE Select	ENSP00000327145.8:n.6004+33_6004+34delinsTG
ENST00000325888.12:c.6004+33_6004+34delinsTG (FLNC)	ENSP00000327145.8:n.6004+33_6004+34delinsTG
ENST00000346177.6:c.5905+33_5905+34delinsTG (FLNC)	ENSP00000344002.6:n.5905+33_5905+34delinsTG
NM_001127487.1:c.5905+33_5905+34delinsTG (FLNC)	NP_001120959.1:n.5905+33_5905+34delinsTG
NM_001458.4:c.6004+33_6004+34delinsTG , LRG_870t1:c.6004+33_6004+34delinsTG (FLNC)	NP_001449.3:n.6004+33_6004+34delinsTG
NR_149055.1:n.215+499_215+500delinsCA (FLNC-AS1)
NM_001127487.2:c.5905+33_5905+34delinsTG (FLNC)	NP_001120959.1:n.5905+33_5905+34delinsTG
NM_001458.5:c.6004+33_6004+34delinsTG (FLNC) MANE Select	NP_001449.3:n.6004+33_6004+34delinsTG