Canonical Allele Identifier: CA2684815709

Gene: FLNC

Linked Data

• gnomAD v4: 7-128849125-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849125_128849126insCA , CM000669.2:g.128849125_128849126insCA	GRCh38
NC_000007.13:g.128489179_128489180insCA , CM000669.1:g.128489179_128489180insCA	GRCh37
NC_000007.12:g.128276415_128276416insCA	NCBI36
NG_011807.1:g.23697_23698insCA , LRG_870:g.23697_23698insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-56_4928-55insCA MANE Select	ENSP00000327145.8:n.4928-56_4928-55insCA
ENST00000325888.12:c.4928-56_4928-55insCA	ENSP00000327145.8:n.4928-56_4928-55insCA
ENST00000346177.6:c.4928-56_4928-55insCA	ENSP00000344002.6:n.4928-56_4928-55insCA
NM_001127487.1:c.4928-56_4928-55insCA	NP_001120959.1:n.4928-56_4928-55insCA
NM_001458.4:c.4928-56_4928-55insCA , LRG_870t1:c.4928-56_4928-55insCA	NP_001449.3:n.4928-56_4928-55insCA
NM_001127487.2:c.4928-56_4928-55insCA	NP_001120959.1:n.4928-56_4928-55insCA
NM_001458.5:c.4928-56_4928-55insCA MANE Select	NP_001449.3:n.4928-56_4928-55insCA