Canonical Allele Identifier: CA2684815604

Gene: FLNC

Linked Data

• gnomAD v4: 7-128849105-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849105_128849106insG , CM000669.2:g.128849105_128849106insG	GRCh38
NC_000007.13:g.128489159_128489160insG , CM000669.1:g.128489159_128489160insG	GRCh37
NC_000007.12:g.128276395_128276396insG	NCBI36
NG_011807.1:g.23677_23678insG , LRG_870:g.23677_23678insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-76_4928-75insG MANE Select	ENSP00000327145.8:n.4928-76_4928-75insG
ENST00000325888.12:c.4928-76_4928-75insG	ENSP00000327145.8:n.4928-76_4928-75insG
ENST00000346177.6:c.4928-76_4928-75insG	ENSP00000344002.6:n.4928-76_4928-75insG
NM_001127487.1:c.4928-76_4928-75insG	NP_001120959.1:n.4928-76_4928-75insG
NM_001458.4:c.4928-76_4928-75insG , LRG_870t1:c.4928-76_4928-75insG	NP_001449.3:n.4928-76_4928-75insG
NM_001127487.2:c.4928-76_4928-75insG	NP_001120959.1:n.4928-76_4928-75insG
NM_001458.5:c.4928-76_4928-75insG MANE Select	NP_001449.3:n.4928-76_4928-75insG