Canonical Allele Identifier: CA4475525

Gene: FLNC

Linked Data

• dbSNP Id: rs772387688
• ExAC: 7:128489362 G / A
• gnomAD v2: 7-128489362-G-A
• gnomAD v4: 7-128849308-G-A
• MyVariant Identifiers: chr7:g.128489362G>A (hg19) ; chr7:g.128849308G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849308G>A , CM000669.2:g.128849308G>A	GRCh38
NC_000007.13:g.128489362G>A , CM000669.1:g.128489362G>A	GRCh37
NC_000007.12:g.128276598G>A	NCBI36
NG_011807.1:g.23880G>A , LRG_870:g.23880G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.4952-23G>A MANE Select	ENSP00000327145.8:n.4952-23G>A
ENST00000325888.12:c.4952-23G>A	ENSP00000327145.8:n.4952-23G>A
ENST00000346177.6:c.4952-23G>A	ENSP00000344002.6:n.4952-23G>A
NM_001127487.1:c.4952-23G>A	NP_001120959.1:n.4952-23G>A
NM_001458.4:c.4952-23G>A , LRG_870t1:c.4952-23G>A	NP_001449.3:n.4952-23G>A
NM_001127487.2:c.4952-23G>A	NP_001120959.1:n.4952-23G>A
NM_001458.5:c.4952-23G>A MANE Select	NP_001449.3:n.4952-23G>A