Canonical Allele Identifier: CA457850034

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1808950190
• COSMIC: COSM3633124
• MyVariant Identifiers: chr7:g.128494221G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128854167G>A , CM000669.2:g.128854167G>A	GRCh38
NC_000007.13:g.128494221G>A , CM000669.1:g.128494221G>A	GRCh37
NC_000007.12:g.128281457G>A	NCBI36
NG_011807.1:g.28739G>A , LRG_870:g.28739G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.6678G>A (FLNC) MANE Select	ENSP00000327145.8:p.Leu2226=
ENST00000325888.12:c.6678G>A (FLNC)	ENSP00000327145.8:p.Leu2226=
ENST00000346177.6:c.6579G>A (FLNC)	ENSP00000344002.6:p.Leu2193=
NM_001127487.1:c.6579G>A (FLNC)	NP_001120959.1:p.Leu2193=
NM_001458.4:c.6678G>A , LRG_870t1:c.6678G>A (FLNC)	NP_001449.3:p.Leu2226=
NR_149055.1:n.103-770C>T (FLNC-AS1)
NM_001127487.2:c.6579G>A (FLNC)	NP_001120959.1:p.Leu2193=
NM_001458.5:c.6678G>A (FLNC) MANE Select	NP_001449.3:p.Leu2226=