Canonical Allele Identifier: CA1742580490

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843345_128843346delinsCT , CM000669.2:g.128843345_128843346delinsCT	GRCh38
NC_000007.13:g.128483399_128483400delinsCT , CM000669.1:g.128483399_128483400delinsCT	GRCh37
NC_000007.12:g.128270635_128270636delinsCT	NCBI36
NG_011807.1:g.17917_17918delinsCT , LRG_870:g.17917_17918delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2641+26_2641+27delinsCT MANE Select	ENSP00000327145.8:n.2641+26_2641+27delinsCT
ENST00000325888.12:c.2641+26_2641+27delinsCT	ENSP00000327145.8:n.2641+26_2641+27delinsCT
ENST00000346177.6:c.2641+26_2641+27delinsCT	ENSP00000344002.6:n.2641+26_2641+27delinsCT
NM_001127487.1:c.2641+26_2641+27delinsCT	NP_001120959.1:n.2641+26_2641+27delinsCT
NM_001458.4:c.2641+26_2641+27delinsCT , LRG_870t1:c.2641+26_2641+27delinsCT	NP_001449.3:n.2641+26_2641+27delinsCT
NM_001127487.2:c.2641+26_2641+27delinsCT	NP_001120959.1:n.2641+26_2641+27delinsCT
NM_001458.5:c.2641+26_2641+27delinsCT MANE Select	NP_001449.3:n.2641+26_2641+27delinsCT