Canonical Allele Identifier: CA1742578487
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853991G= , CM000669.2:g.128853991G= GRCh38
NC_000007.13:g.128494045G= , CM000669.1:g.128494045G= GRCh37
NC_000007.12:g.128281281G= NCBI36
NG_011807.1:g.28563G= , LRG_870:g.28563G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6502G= (FLNC) MANE Select ENSP00000327145.8:p.Val2168=
ENST00000325888.12:c.6502G= (FLNC) ENSP00000327145.8:p.Val2168=
ENST00000346177.6:c.6403G= (FLNC) ENSP00000344002.6:p.Val2135=
NM_001127487.1:c.6403G= (FLNC) NP_001120959.1:p.Val2135=
NM_001458.4:c.6502G= , LRG_870t1:c.6502G= (FLNC) NP_001449.3:p.Val2168=
NR_149055.1:n.103-594C= (FLNC-AS1)
NM_001127487.2:c.6403G= (FLNC) NP_001120959.1:p.Val2135=
NM_001458.5:c.6502G= (FLNC) MANE Select NP_001449.3:p.Val2168=