Canonical Allele Identifier: CA369210891
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2585967
ClinVar RCV Id: RCV003368110

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852834C>T , CM000669.2:g.128852834C>T GRCh38
NC_000007.13:g.128492888C>T , CM000669.1:g.128492888C>T GRCh37
NC_000007.12:g.128280124C>T NCBI36
NG_011807.1:g.27406C>T , LRG_870:g.27406C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6011C>T (FLNC) MANE Select ENSP00000327145.8:p.Ser2004Phe
ENST00000325888.12:c.6011C>T (FLNC) ENSP00000327145.8:p.Ser2004Phe
ENST00000346177.6:c.5912C>T (FLNC) ENSP00000344002.6:p.Ser1971Phe
NM_001127487.1:c.5912C>T (FLNC) NP_001120959.1:p.Ser1971Phe
NM_001458.4:c.6011C>T , LRG_870t1:c.6011C>T (FLNC) NP_001449.3:p.Ser2004Phe
NR_149055.1:n.215+451G>A (FLNC-AS1)
NM_001127487.2:c.5912C>T (FLNC) NP_001120959.1:p.Ser1971Phe
NM_001458.5:c.6011C>T (FLNC) MANE Select NP_001449.3:p.Ser2004Phe