Canonical Allele Identifier: CA2684817050
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128855111G>A , CM000669.2:g.128855111G>A GRCh38
NC_000007.13:g.128495165G>A , CM000669.1:g.128495165G>A GRCh37
NC_000007.12:g.128282401G>A NCBI36
NG_011807.1:g.29683G>A , LRG_870:g.29683G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7136-88G>A (FLNC) MANE Select ENSP00000327145.8:n.7136-88G>A
ENST00000325888.12:c.7136-88G>A (FLNC) ENSP00000327145.8:n.7136-88G>A
ENST00000346177.6:c.7037-88G>A (FLNC) ENSP00000344002.6:n.7037-88G>A
NM_001127487.1:c.7037-88G>A (FLNC) NP_001120959.1:n.7037-88G>A
NM_001458.4:c.7136-88G>A , LRG_870t1:c.7136-88G>A (FLNC) NP_001449.3:n.7136-88G>A
NR_149055.1:n.103-1714C>T (FLNC-AS1)
NM_001127487.2:c.7037-88G>A (FLNC) NP_001120959.1:n.7037-88G>A
NM_001458.5:c.7136-88G>A (FLNC) MANE Select NP_001449.3:n.7136-88G>A