Canonical Allele Identifier: CA457849251

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1474848200
• gnomAD v2: 7-128491456-A-G
• gnomAD v4: 7-128851402-A-G
• MyVariant Identifiers: chr7:g.128491456A>G (hg19) ; chr7:g.128851402A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128851402A>G , CM000669.2:g.128851402A>G	GRCh38
NC_000007.13:g.128491456A>G , CM000669.1:g.128491456A>G	GRCh37
NC_000007.12:g.128278692A>G	NCBI36
NG_011807.1:g.25974A>G , LRG_870:g.25974A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.5668+42A>G (FLNC) MANE Select	ENSP00000327145.8:n.5668+42A>G
ENST00000325888.12:c.5668+42A>G (FLNC)	ENSP00000327145.8:n.5668+42A>G
ENST00000346177.6:c.5569+42A>G (FLNC)	ENSP00000344002.6:n.5569+42A>G
NM_001127487.1:c.5569+42A>G (FLNC)	NP_001120959.1:n.5569+42A>G
NM_001458.4:c.5668+42A>G , LRG_870t1:c.5668+42A>G (FLNC)	NP_001449.3:n.5668+42A>G
NR_149055.1:n.314T>C (FLNC-AS1)
NM_001127487.2:c.5569+42A>G (FLNC)	NP_001120959.1:n.5569+42A>G
NM_001458.5:c.5668+42A>G (FLNC) MANE Select	NP_001449.3:n.5668+42A>G