Canonical Allele Identifier: CA4475259
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472062
dbSNP Id: rs183668401

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128846757C>T , CM000669.2:g.128846757C>T GRCh38
NC_000007.13:g.128486811C>T , CM000669.1:g.128486811C>T GRCh37
NC_000007.12:g.128274047C>T NCBI36
NG_011807.1:g.21329C>T , LRG_870:g.21329C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4140C>T MANE Select ENSP00000327145.8:p.Thr1380=
ENST00000325888.12:c.4140C>T ENSP00000327145.8:p.Thr1380=
ENST00000346177.6:c.4140C>T ENSP00000344002.6:p.Thr1380=
NM_001127487.1:c.4140C>T NP_001120959.1:p.Thr1380=
NM_001458.4:c.4140C>T , LRG_870t1:c.4140C>T NP_001449.3:p.Thr1380=
NM_001127487.2:c.4140C>T NP_001120959.1:p.Thr1380=
NM_001458.5:c.4140C>T MANE Select NP_001449.3:p.Thr1380=