Canonical Allele Identifier: CA166214269

Gene: FLNC

Linked Data

• ClinVar Variation Id: 2420698
• ClinVar RCV Id: RCV003121863
• dbSNP Id: rs755636271
• gnomAD v4: 7-128837394-G-A
• MyVariant Identifiers: chr7:g.128837394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128837394G>A , CM000669.2:g.128837394G>A	GRCh38
NC_000007.13:g.128477448G>A , CM000669.1:g.128477448G>A	GRCh37
NC_000007.12:g.128264684G>A	NCBI36
NG_011807.1:g.11966G>A , LRG_870:g.11966G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.700-4G>A MANE Select	ENSP00000327145.8:n.700-4G>A
ENST00000325888.12:c.700-4G>A	ENSP00000327145.8:n.700-4G>A
ENST00000346177.6:c.700-4G>A	ENSP00000344002.6:n.700-4G>A
NM_001127487.1:c.700-4G>A	NP_001120959.1:n.700-4G>A
NM_001458.4:c.700-4G>A , LRG_870t1:c.700-4G>A	NP_001449.3:n.700-4G>A
NM_001127487.2:c.700-4G>A	NP_001120959.1:n.700-4G>A
NM_001458.5:c.700-4G>A MANE Select	NP_001449.3:n.700-4G>A