Canonical Allele Identifier: CA1742581070

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843607_128843608delinsCG , CM000669.2:g.128843607_128843608delinsCG	GRCh38
NC_000007.13:g.128483661_128483662delinsCG , CM000669.1:g.128483661_128483662delinsCG	GRCh37
NC_000007.12:g.128270897_128270898delinsCG	NCBI36
NG_011807.1:g.18179_18180delinsCG , LRG_870:g.18179_18180delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2811+30_2811+31delinsCG MANE Select	ENSP00000327145.8:n.2811+30_2811+31delinsCG
ENST00000325888.12:c.2811+30_2811+31delinsCG	ENSP00000327145.8:n.2811+30_2811+31delinsCG
ENST00000346177.6:c.2811+30_2811+31delinsCG	ENSP00000344002.6:n.2811+30_2811+31delinsCG
NM_001127487.1:c.2811+30_2811+31delinsCG	NP_001120959.1:n.2811+30_2811+31delinsCG
NM_001458.4:c.2811+30_2811+31delinsCG , LRG_870t1:c.2811+30_2811+31delinsCG	NP_001449.3:n.2811+30_2811+31delinsCG
NM_001127487.2:c.2811+30_2811+31delinsCG	NP_001120959.1:n.2811+30_2811+31delinsCG
NM_001458.5:c.2811+30_2811+31delinsCG MANE Select	NP_001449.3:n.2811+30_2811+31delinsCG