Canonical Allele Identifier: CA369211248
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2100994
ClinVar RCV Id: RCV003033633

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852929T>G , CM000669.2:g.128852929T>G GRCh38
NC_000007.13:g.128492983T>G , CM000669.1:g.128492983T>G GRCh37
NC_000007.12:g.128280219T>G NCBI36
NG_011807.1:g.27501T>G , LRG_870:g.27501T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6106T>G (FLNC) MANE Select ENSP00000327145.8:p.Ser2036Ala
ENST00000325888.12:c.6106T>G (FLNC) ENSP00000327145.8:p.Ser2036Ala
ENST00000346177.6:c.6007T>G (FLNC) ENSP00000344002.6:p.Ser2003Ala
NM_001127487.1:c.6007T>G (FLNC) NP_001120959.1:p.Ser2003Ala
NM_001458.4:c.6106T>G , LRG_870t1:c.6106T>G (FLNC) NP_001449.3:p.Ser2036Ala
NR_149055.1:n.215+356A>C (FLNC-AS1)
NM_001127487.2:c.6007T>G (FLNC) NP_001120959.1:p.Ser2003Ala
NM_001458.5:c.6106T>G (FLNC) MANE Select NP_001449.3:p.Ser2036Ala