Canonical Allele Identifier: CA166217166

Gene: FLNC

Linked Data

• dbSNP Id: rs1057154204
• MyVariant Identifiers: chr7:g.128481294del (hg19) ; chr7:g.128841240del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841240del , CM000669.2:g.128841240del	GRCh38
NC_000007.13:g.128481294del , CM000669.1:g.128481294del	GRCh37
NC_000007.12:g.128268530del	NCBI36
NG_011807.1:g.15812del , LRG_870:g.15812del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1884del MANE Select	ENSP00000327145.8:p.Arg629GlyfsTer?
ENST00000325888.12:c.1884del	ENSP00000327145.8:p.Arg629GlyfsTer?
ENST00000346177.6:c.1884del	ENSP00000344002.6:p.Arg629GlyfsTer?
NM_001127487.1:c.1884del	NP_001120959.1:p.Arg629GlyfsTer?
NM_001458.4:c.1884del , LRG_870t1:c.1884del	NP_001449.3:p.Arg629GlyfsTer?
NM_001127487.2:c.1884del	NP_001120959.1:p.Arg629GlyfsTer?
NM_001458.5:c.1884del MANE Select	NP_001449.3:p.Arg629GlyfsTer?