Canonical Allele Identifier: CA2684820388

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs2128940436
• gnomAD v4: 7-128857429-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857429C>T , CM000669.2:g.128857429C>T	GRCh38
NC_000007.13:g.128497483C>T , CM000669.1:g.128497483C>T	GRCh37
NC_000007.12:g.128284719C>T	NCBI36
NG_011807.1:g.32001C>T , LRG_870:g.32001C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+93C>T (FLNC) MANE Select	ENSP00000327145.8:n.7780+93C>T
ENST00000325888.12:c.7780+93C>T (FLNC)	ENSP00000327145.8:n.7780+93C>T
ENST00000346177.6:c.7681+93C>T (FLNC)	ENSP00000344002.6:n.7681+93C>T
NM_001127487.1:c.7681+93C>T (FLNC)	NP_001120959.1:n.7681+93C>T
NM_001458.4:c.7780+93C>T , LRG_870t1:c.7780+93C>T (FLNC)	NP_001449.3:n.7780+93C>T
NR_149055.1:n.103-4032G>A (FLNC-AS1)
NM_001127487.2:c.7681+93C>T (FLNC)	NP_001120959.1:n.7681+93C>T
NM_001458.5:c.7780+93C>T (FLNC) MANE Select	NP_001449.3:n.7780+93C>T