Canonical Allele Identifier: CA2579014412

Gene: FLNC

Linked Data

• gnomAD v4: 7-128849116-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849120_128849121dup , CM000669.2:g.128849120_128849121dup	GRCh38
NC_000007.13:g.128489174_128489175dup , CM000669.1:g.128489174_128489175dup	GRCh37
NC_000007.12:g.128276410_128276411dup	NCBI36
NG_011807.1:g.23692_23693dup , LRG_870:g.23692_23693dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-61_4928-60dup MANE Select	ENSP00000327145.8:n.4928-61_4928-60dup
ENST00000325888.12:c.4928-61_4928-60dup	ENSP00000327145.8:n.4928-61_4928-60dup
ENST00000346177.6:c.4928-61_4928-60dup	ENSP00000344002.6:n.4928-61_4928-60dup
NM_001127487.1:c.4928-61_4928-60dup	NP_001120959.1:n.4928-61_4928-60dup
NM_001458.4:c.4928-61_4928-60dup , LRG_870t1:c.4928-61_4928-60dup	NP_001449.3:n.4928-61_4928-60dup
NM_001127487.2:c.4928-61_4928-60dup	NP_001120959.1:n.4928-61_4928-60dup
NM_001458.5:c.4928-61_4928-60dup MANE Select	NP_001449.3:n.4928-61_4928-60dup