Canonical Allele Identifier: CA369211272

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 1447193
• ClinVar RCV Id: RCV001996734
• dbSNP Id: rs559639511
• MyVariant Identifiers: chr7:g.128492991C>G (hg19) ; chr7:g.128852937C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128852937C>G , CM000669.2:g.128852937C>G	GRCh38
NC_000007.13:g.128492991C>G , CM000669.1:g.128492991C>G	GRCh37
NC_000007.12:g.128280227C>G	NCBI36
NG_011807.1:g.27509C>G , LRG_870:g.27509C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6114C>G (FLNC) MANE Select	ENSP00000327145.8:p.Ile2038Met
ENST00000325888.12:c.6114C>G (FLNC)	ENSP00000327145.8:p.Ile2038Met
ENST00000346177.6:c.6015C>G (FLNC)	ENSP00000344002.6:p.Ile2005Met
NM_001127487.1:c.6015C>G (FLNC)	NP_001120959.1:p.Ile2005Met
NM_001458.4:c.6114C>G , LRG_870t1:c.6114C>G (FLNC)	NP_001449.3:p.Ile2038Met
NR_149055.1:n.215+348G>C (FLNC-AS1)
NM_001127487.2:c.6015C>G (FLNC)	NP_001120959.1:p.Ile2005Met
NM_001458.5:c.6114C>G (FLNC) MANE Select	NP_001449.3:p.Ile2038Met