Canonical Allele Identifier: CA2684820560

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128857992-TCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857995_128857997del , CM000669.2:g.128857995_128857997del	GRCh38
NC_000007.13:g.128498049_128498051del , CM000669.1:g.128498049_128498051del	GRCh37
NC_000007.12:g.128285285_128285287del	NCBI36
NG_011807.1:g.32567_32569del , LRG_870:g.32567_32569del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7781-13_7781-11del (FLNC) MANE Select	ENSP00000327145.8:n.7781-13_7781-11del
ENST00000325888.12:c.7781-13_7781-11del (FLNC)	ENSP00000327145.8:n.7781-13_7781-11del
ENST00000346177.6:c.7682-13_7682-11del (FLNC)	ENSP00000344002.6:n.7682-13_7682-11del
NM_001127487.1:c.7682-13_7682-11del (FLNC)	NP_001120959.1:n.7682-13_7682-11del
NM_001458.4:c.7781-13_7781-11del , LRG_870t1:c.7781-13_7781-11del (FLNC)	NP_001449.3:n.7781-13_7781-11del
NR_149055.1:n.102+4530_102+4532del (FLNC-AS1)
NM_001127487.2:c.7682-13_7682-11del (FLNC)	NP_001120959.1:n.7682-13_7682-11del
NM_001458.5:c.7781-13_7781-11del (FLNC) MANE Select	NP_001449.3:n.7781-13_7781-11del