Canonical Allele Identifier: CA2684816312

Gene: FLNC

Linked Data

• gnomAD v4: 7-128843736-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843738del , CM000669.2:g.128843738del	GRCh38
NC_000007.13:g.128483792del , CM000669.1:g.128483792del	GRCh37
NC_000007.12:g.128271028del	NCBI36
NG_011807.1:g.18310del , LRG_870:g.18310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2812-58del MANE Select	ENSP00000327145.8:n.2812-58del
ENST00000325888.12:c.2812-58del	ENSP00000327145.8:n.2812-58del
ENST00000346177.6:c.2812-58del	ENSP00000344002.6:n.2812-58del
NM_001127487.1:c.2812-58del	NP_001120959.1:n.2812-58del
NM_001458.4:c.2812-58del , LRG_870t1:c.2812-58del	NP_001449.3:n.2812-58del
NM_001127487.2:c.2812-58del	NP_001120959.1:n.2812-58del
NM_001458.5:c.2812-58del MANE Select	NP_001449.3:n.2812-58del