Canonical Allele Identifier: CA4474708

Gene: FLNC

Linked Data

• dbSNP Id: rs770333344
• ExAC: 7:128482805 CG / C
• gnomAD v2: 7-128482805-CG-C
• gnomAD v4: 7-128842751-CG-C
• MyVariant Identifiers: chr7:g.128482806del (hg19) ; chr7:g.128842752del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128842756del , CM000669.2:g.128842756del	GRCh38
NC_000007.13:g.128482810del , CM000669.1:g.128482810del	GRCh37
NC_000007.12:g.128270046del	NCBI36
NG_011807.1:g.17328del , LRG_870:g.17328del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.2390-38del MANE Select	ENSP00000327145.8:n.2390-38del
ENST00000325888.12:c.2390-38del	ENSP00000327145.8:n.2390-38del
ENST00000346177.6:c.2390-38del	ENSP00000344002.6:n.2390-38del
ENST00000388853.3:n.506-38del
NM_001127487.1:c.2390-38del	NP_001120959.1:n.2390-38del
NM_001458.4:c.2390-38del , LRG_870t1:c.2390-38del	NP_001449.3:n.2390-38del
NM_001127487.2:c.2390-38del	NP_001120959.1:n.2390-38del
NM_001458.5:c.2390-38del MANE Select	NP_001449.3:n.2390-38del