Canonical Allele Identifier: CA166175372

Gene: FLNC

Linked Data

• dbSNP Id: rs35978387
• MyVariant Identifiers: chr7:g.128482815del (hg19) ; chr7:g.128842761del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128842761del , CM000669.2:g.128842761del	GRCh38
NC_000007.13:g.128482815del , CM000669.1:g.128482815del	GRCh37
NC_000007.12:g.128270051del	NCBI36
NG_011807.1:g.17333del , LRG_870:g.17333del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.2390-33del MANE Select	ENSP00000327145.8:n.2390-33del
ENST00000325888.12:c.2390-33del	ENSP00000327145.8:n.2390-33del
ENST00000346177.6:c.2390-33del	ENSP00000344002.6:n.2390-33del
ENST00000388853.3:n.506-33del
NM_001127487.1:c.2390-33del	NP_001120959.1:n.2390-33del
NM_001458.4:c.2390-33del , LRG_870t1:c.2390-33del	NP_001449.3:n.2390-33del
NM_001127487.2:c.2390-33del	NP_001120959.1:n.2390-33del
NM_001458.5:c.2390-33del MANE Select	NP_001449.3:n.2390-33del