Canonical Allele Identifier: CA2684820160

Gene: FLNC

Linked Data

• gnomAD v4: 7-128839934-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128839938dup , CM000669.2:g.128839938dup	GRCh38
NC_000007.13:g.128479992dup , CM000669.1:g.128479992dup	GRCh37
NC_000007.12:g.128267228dup	NCBI36
NG_011807.1:g.14510dup , LRG_870:g.14510dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1412-85dup MANE Select	ENSP00000327145.8:n.1412-85dup
ENST00000325888.12:c.1412-85dup	ENSP00000327145.8:n.1412-85dup
ENST00000346177.6:c.1412-85dup	ENSP00000344002.6:n.1412-85dup
NM_001127487.1:c.1412-85dup	NP_001120959.1:n.1412-85dup
NM_001458.4:c.1412-85dup , LRG_870t1:c.1412-85dup	NP_001449.3:n.1412-85dup
NM_001127487.2:c.1412-85dup	NP_001120959.1:n.1412-85dup
NM_001458.5:c.1412-85dup MANE Select	NP_001449.3:n.1412-85dup