Canonical Allele Identifier: CA2580076535

Gene: FLNC

Linked Data

• ClinVar Variation Id: 2441494
• ClinVar RCV Id: RCV003144035

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849178del , CM000669.2:g.128849178del	GRCh38
NC_000007.13:g.128489232del , CM000669.1:g.128489232del	GRCh37
NC_000007.12:g.128276468del	NCBI36
NG_011807.1:g.23750del , LRG_870:g.23750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4928-3del MANE Select	ENSP00000327145.8:n.4928-3del
ENST00000325888.12:c.4928-3del	ENSP00000327145.8:n.4928-3del
ENST00000346177.6:c.4928-3del	ENSP00000344002.6:n.4928-3del
NM_001127487.1:c.4928-3del	NP_001120959.1:n.4928-3del
NM_001458.4:c.4928-3del , LRG_870t1:c.4928-3del	NP_001449.3:n.4928-3del
NM_001127487.2:c.4928-3del	NP_001120959.1:n.4928-3del
NM_001458.5:c.4928-3del MANE Select	NP_001449.3:n.4928-3del