Canonical Allele Identifier: CA369211247
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6106T>A (FLNC) MANE Select ENSP00000327145.8:p.Ser2036Thr
ENST00000325888.12:c.6106T>A (FLNC) ENSP00000327145.8:p.Ser2036Thr
ENST00000346177.6:c.6007T>A (FLNC) ENSP00000344002.6:p.Ser2003Thr
NM_001127487.1:c.6007T>A (FLNC) NP_001120959.1:p.Ser2003Thr
NM_001458.4:c.6106T>A , LRG_870t1:c.6106T>A (FLNC) NP_001449.3:p.Ser2036Thr
NR_149055.1:n.215+356A>T (FLNC-AS1)
NM_001127487.2:c.6007T>A (FLNC) NP_001120959.1:p.Ser2003Thr
NM_001458.5:c.6106T>A (FLNC) MANE Select NP_001449.3:p.Ser2036Thr