Canonical Allele Identifier: CA4475545
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472084
dbSNP Id: rs374124083

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849399G>A , CM000669.2:g.128849399G>A GRCh38
NC_000007.13:g.128489453G>A , CM000669.1:g.128489453G>A GRCh37
NC_000007.12:g.128276689G>A NCBI36
NG_011807.1:g.23971G>A , LRG_870:g.23971G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5020G>A MANE Select ENSP00000327145.8:p.Gly1674Ser
ENST00000325888.12:c.5020G>A ENSP00000327145.8:p.Gly1674Ser
ENST00000346177.6:c.5020G>A ENSP00000344002.6:p.Gly1674Ser
NM_001127487.1:c.5020G>A NP_001120959.1:p.Gly1674Ser
NM_001458.4:c.5020G>A , LRG_870t1:c.5020G>A NP_001449.3:p.Gly1674Ser
NM_001127487.2:c.5020G>A NP_001120959.1:p.Gly1674Ser
NM_001458.5:c.5020G>A MANE Select NP_001449.3:p.Gly1674Ser