Canonical Allele Identifier: CA1742585231

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128845163_128845164delinsAT , CM000669.2:g.128845163_128845164delinsAT	GRCh38
NC_000007.13:g.128485217_128485218delinsAT , CM000669.1:g.128485217_128485218delinsAT	GRCh37
NC_000007.12:g.128272453_128272454delinsAT	NCBI36
NG_011807.1:g.19735_19736delinsAT , LRG_870:g.19735_19736delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.3698_3699delinsAT MANE Select	ENSP00000327145.8:p.His1233=
ENST00000325888.12:c.3698_3699delinsAT	ENSP00000327145.8:p.His1233=
ENST00000346177.6:c.3698_3699delinsAT	ENSP00000344002.6:p.His1233=
NM_001127487.1:c.3698_3699delinsAT	NP_001120959.1:p.His1233=
NM_001458.4:c.3698_3699delinsAT , LRG_870t1:c.3698_3699delinsAT	NP_001449.3:p.His1233=
NM_001127487.2:c.3698_3699delinsAT	NP_001120959.1:p.His1233=
NM_001458.5:c.3698_3699delinsAT MANE Select	NP_001449.3:p.His1233=