Canonical Allele Identifier: CA1742552717
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1809173781

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858581_128858582insGA , CM000669.2:g.128858581_128858582insGA GRCh38
NC_000007.13:g.128498635_128498636insGA , CM000669.1:g.128498635_128498636insGA GRCh37
NC_000007.12:g.128285871_128285872insGA NCBI36
NG_011807.1:g.33153_33154insGA , LRG_870:g.33153_33154insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*58_*59insGA (FLNC) MANE Select ENSP00000327145.8:n.*58_*59insGA
ENST00000325888.12:c.*58_*59insGA (FLNC) ENSP00000327145.8:n.*58_*59insGA
ENST00000346177.6:c.*58_*59insGA (FLNC) ENSP00000344002.6:n.*58_*59insGA
NM_001127487.1:c.*58_*59insGA (FLNC) NP_001120959.1:n.*58_*59insGA
NM_001458.4:c.*58_*59insGA , LRG_870t1:c.*58_*59insGA (FLNC) NP_001449.3:n.*58_*59insGA
NR_149055.1:n.102+3944_102+3945insCT (FLNC-AS1)
NM_001127487.2:c.*58_*59insGA (FLNC) NP_001120959.1:n.*58_*59insGA
NM_001458.5:c.*58_*59insGA (FLNC) MANE Select NP_001449.3:n.*58_*59insGA