Canonical Allele Identifier: CA2840046314

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128847785_128847786del , CM000669.2:g.128847785_128847786del	GRCh38
NC_000007.13:g.128487839_128487840del , CM000669.1:g.128487839_128487840del	GRCh37
NC_000007.12:g.128275075_128275076del	NCBI36
NG_011807.1:g.22357_22358del , LRG_870:g.22357_22358del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4377_4378del MANE Select	ENSP00000327145.8:p.Arg1460GlyfsTer?
ENST00000325888.12:c.4377_4378del	ENSP00000327145.8:p.Arg1460GlyfsTer?
ENST00000346177.6:c.4377_4378del	ENSP00000344002.6:p.Arg1460GlyfsTer?
NM_001127487.1:c.4377_4378del	NP_001120959.1:p.Arg1460GlyfsTer?
NM_001458.4:c.4377_4378del , LRG_870t1:c.4377_4378del	NP_001449.3:p.Arg1460GlyfsTer?
NM_001127487.2:c.4377_4378del	NP_001120959.1:p.Arg1460GlyfsTer?
NM_001458.5:c.4377_4378del MANE Select	NP_001449.3:p.Arg1460GlyfsTer?