Canonical Allele Identifier: CA2695203137

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128835326del , CM000669.2:g.128835326del	GRCh38
NC_000007.13:g.128475380del , CM000669.1:g.128475380del	GRCh37
NC_000007.12:g.128262616del	NCBI36
NG_011807.1:g.9898del , LRG_870:g.9898del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.353del MANE Select	ENSP00000327145.8:p.Asp118AlafsTer10
ENST00000325888.12:c.353del	ENSP00000327145.8:p.Asp118AlafsTer10
ENST00000346177.6:c.353del	ENSP00000344002.6:p.Asp118AlafsTer10
NM_001127487.1:c.353del	NP_001120959.1:p.Asp118AlafsTer10
NM_001458.4:c.353del , LRG_870t1:c.353del	NP_001449.3:p.Asp118AlafsTer10
NM_001127487.2:c.353del	NP_001120959.1:p.Asp118AlafsTer10
NM_001458.5:c.353del MANE Select	NP_001449.3:p.Asp118AlafsTer10