Canonical Allele Identifier: CA369192213

Gene: FLNC

Linked Data

• dbSNP Id: rs1487853896
• gnomAD v2: 7-128483296-G-A
• gnomAD v4: 7-128843242-G-A
• MyVariant Identifiers: chr7:g.128483296G>A (hg19) ; chr7:g.128843242G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128843242G>A , CM000669.2:g.128843242G>A	GRCh38
NC_000007.13:g.128483296G>A , CM000669.1:g.128483296G>A	GRCh37
NC_000007.12:g.128270532G>A	NCBI36
NG_011807.1:g.17814G>A , LRG_870:g.17814G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.2564G>A MANE Select	ENSP00000327145.8:p.Ser855Asn
ENST00000325888.12:c.2564G>A	ENSP00000327145.8:p.Ser855Asn
ENST00000346177.6:c.2564G>A	ENSP00000344002.6:p.Ser855Asn
NM_001127487.1:c.2564G>A	NP_001120959.1:p.Ser855Asn
NM_001458.4:c.2564G>A , LRG_870t1:c.2564G>A	NP_001449.3:p.Ser855Asn
NM_001127487.2:c.2564G>A	NP_001120959.1:p.Ser855Asn
NM_001458.5:c.2564G>A MANE Select	NP_001449.3:p.Ser855Asn