Canonical Allele Identifier: CA4475515

Gene: FLNC

Linked Data

• dbSNP Id: rs769007790
• ExAC: 7:128489288 GT / G
• gnomAD v3: 7-128849234-GT-G
• gnomAD v4: 7-128849234-GT-G
• MyVariant Identifiers: chr7:g.128489289del (hg19) ; chr7:g.128849235del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849235del , CM000669.2:g.128849235del	GRCh38
NC_000007.13:g.128489289del , CM000669.1:g.128489289del	GRCh37
NC_000007.12:g.128276525del	NCBI36
NG_011807.1:g.23807del , LRG_870:g.23807del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4951+31del MANE Select	ENSP00000327145.8:n.4951+31del
ENST00000325888.12:c.4951+31del	ENSP00000327145.8:n.4951+31del
ENST00000346177.6:c.4951+31del	ENSP00000344002.6:n.4951+31del
NM_001127487.1:c.4951+31del	NP_001120959.1:n.4951+31del
NM_001458.4:c.4951+31del , LRG_870t1:c.4951+31del	NP_001449.3:n.4951+31del
NM_001127487.2:c.4951+31del	NP_001120959.1:n.4951+31del
NM_001458.5:c.4951+31del MANE Select	NP_001449.3:n.4951+31del