Canonical Allele Identifier: CA10607003
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 291057
ClinVar RCV Id: RCV002429239
dbSNP Id: rs886044638
gnomAD v4: 7-128842863-A-T
MyVariant Identifiers: chr7:g.128482917A>T (hg19) chr7:g.128842863A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842863A>T , CM000669.2:g.128842863A>T GRCh38
NC_000007.13:g.128482917A>T , CM000669.1:g.128482917A>T GRCh37
NC_000007.12:g.128270153A>T NCBI36
NG_011807.1:g.17435A>T , LRG_870:g.17435A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2459A>T MANE Select ENSP00000327145.8:p.Asp820Val
ENST00000325888.12:c.2459A>T ENSP00000327145.8:p.Asp820Val
ENST00000346177.6:c.2459A>T ENSP00000344002.6:p.Asp820Val
NM_001127487.1:c.2459A>T NP_001120959.1:p.Asp820Val
NM_001458.4:c.2459A>T , LRG_870t1:c.2459A>T NP_001449.3:p.Asp820Val
NM_001127487.2:c.2459A>T NP_001120959.1:p.Asp820Val
NM_001458.5:c.2459A>T MANE Select NP_001449.3:p.Asp820Val
Search 100 bp 5'
Search 100 bp 3'