Canonical Allele Identifier: CA2684815478

Gene: FLNC

Linked Data

• gnomAD v4: 7-128843132-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843132C>A , CM000669.2:g.128843132C>A	GRCh38
NC_000007.13:g.128483186C>A , CM000669.1:g.128483186C>A	GRCh37
NC_000007.12:g.128270422C>A	NCBI36
NG_011807.1:g.17704C>A , LRG_870:g.17704C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2551-97C>A MANE Select	ENSP00000327145.8:n.2551-97C>A
ENST00000325888.12:c.2551-97C>A	ENSP00000327145.8:n.2551-97C>A
ENST00000346177.6:c.2551-97C>A	ENSP00000344002.6:n.2551-97C>A
NM_001127487.1:c.2551-97C>A	NP_001120959.1:n.2551-97C>A
NM_001458.4:c.2551-97C>A , LRG_870t1:c.2551-97C>A	NP_001449.3:n.2551-97C>A
NM_001127487.2:c.2551-97C>A	NP_001120959.1:n.2551-97C>A
NM_001458.5:c.2551-97C>A MANE Select	NP_001449.3:n.2551-97C>A