Canonical Allele Identifier: CA2573049002

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128847847_128847853del , CM000669.2:g.128847847_128847853del	GRCh38
NC_000007.13:g.128487901_128487907del , CM000669.1:g.128487901_128487907del	GRCh37
NC_000007.12:g.128275137_128275143del	NCBI36
NG_011807.1:g.22419_22425del , LRG_870:g.22419_22425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4439_4445del MANE Select	ENSP00000327145.8:p.Ala1480GlyfsTer?
ENST00000325888.12:c.4439_4445del	ENSP00000327145.8:p.Ala1480GlyfsTer?
ENST00000346177.6:c.4439_4445del	ENSP00000344002.6:p.Ala1480GlyfsTer?
NM_001127487.1:c.4439_4445del	NP_001120959.1:p.Ala1480GlyfsTer?
NM_001458.4:c.4439_4445del , LRG_870t1:c.4439_4445del	NP_001449.3:p.Ala1480GlyfsTer?
NM_001127487.2:c.4439_4445del	NP_001120959.1:p.Ala1480GlyfsTer?
NM_001458.5:c.4439_4445del MANE Select	NP_001449.3:p.Ala1480GlyfsTer?