Canonical Allele Identifier: CA1742575288

Gene: FLNC FLNC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128852779_128852780delinsCA , CM000669.2:g.128852779_128852780delinsCA	GRCh38
NC_000007.13:g.128492833_128492834delinsCA , CM000669.1:g.128492833_128492834delinsCA	GRCh37
NC_000007.12:g.128280069_128280070delinsCA	NCBI36
NG_011807.1:g.27351_27352delinsCA , LRG_870:g.27351_27352delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6004+27_6004+28delinsCA (FLNC) MANE Select	ENSP00000327145.8:n.6004+27_6004+28delinsCA
ENST00000325888.12:c.6004+27_6004+28delinsCA (FLNC)	ENSP00000327145.8:n.6004+27_6004+28delinsCA
ENST00000346177.6:c.5905+27_5905+28delinsCA (FLNC)	ENSP00000344002.6:n.5905+27_5905+28delinsCA
NM_001127487.1:c.5905+27_5905+28delinsCA (FLNC)	NP_001120959.1:n.5905+27_5905+28delinsCA
NM_001458.4:c.6004+27_6004+28delinsCA , LRG_870t1:c.6004+27_6004+28delinsCA (FLNC)	NP_001449.3:n.6004+27_6004+28delinsCA
NR_149055.1:n.215+505_215+506delinsTG (FLNC-AS1)
NM_001127487.2:c.5905+27_5905+28delinsCA (FLNC)	NP_001120959.1:n.5905+27_5905+28delinsCA
NM_001458.5:c.6004+27_6004+28delinsCA (FLNC) MANE Select	NP_001449.3:n.6004+27_6004+28delinsCA