Canonical Allele Identifier: CA833136006

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1488176375
• gnomAD v4: 7-128857366-A-T
• MyVariant Identifiers: chr7:g.128497420A>T (hg19) ; chr7:g.128857366A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857366A>T , CM000669.2:g.128857366A>T	GRCh38
NC_000007.13:g.128497420A>T , CM000669.1:g.128497420A>T	GRCh37
NC_000007.12:g.128284656A>T	NCBI36
NG_011807.1:g.31938A>T , LRG_870:g.31938A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+30A>T (FLNC) MANE Select	ENSP00000327145.8:n.7780+30A>T
ENST00000325888.12:c.7780+30A>T (FLNC)	ENSP00000327145.8:n.7780+30A>T
ENST00000346177.6:c.7681+30A>T (FLNC)	ENSP00000344002.6:n.7681+30A>T
NM_001127487.1:c.7681+30A>T (FLNC)	NP_001120959.1:n.7681+30A>T
NM_001458.4:c.7780+30A>T , LRG_870t1:c.7780+30A>T (FLNC)	NP_001449.3:n.7780+30A>T
NR_149055.1:n.103-3969T>A (FLNC-AS1)
NM_001127487.2:c.7681+30A>T (FLNC)	NP_001120959.1:n.7681+30A>T
NM_001458.5:c.7780+30A>T (FLNC) MANE Select	NP_001449.3:n.7780+30A>T