Canonical Allele Identifier: CA2684812752

Gene: FLNC

Linked Data

• gnomAD v4: 7-128841181-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841182del , CM000669.2:g.128841182del	GRCh38
NC_000007.13:g.128481236del , CM000669.1:g.128481236del	GRCh37
NC_000007.12:g.128268472del	NCBI36
NG_011807.1:g.15754del , LRG_870:g.15754del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1826del MANE Select	ENSP00000327145.8:p.Glu609GlyfsTer?
ENST00000325888.12:c.1826del	ENSP00000327145.8:p.Glu609GlyfsTer?
ENST00000346177.6:c.1826del	ENSP00000344002.6:p.Glu609GlyfsTer?
NM_001127487.1:c.1826del	NP_001120959.1:p.Glu609GlyfsTer?
NM_001458.4:c.1826del , LRG_870t1:c.1826del	NP_001449.3:p.Glu609GlyfsTer?
NM_001127487.2:c.1826del	NP_001120959.1:p.Glu609GlyfsTer?
NM_001458.5:c.1826del MANE Select	NP_001449.3:p.Glu609GlyfsTer?