Canonical Allele Identifier: CA652180309
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1809174427

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858594C>A , CM000669.2:g.128858594C>A GRCh38
NC_000007.13:g.128498648C>A , CM000669.1:g.128498648C>A GRCh37
NC_000007.12:g.128285884C>A NCBI36
NG_011807.1:g.33166C>A , LRG_870:g.33166C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*71C>A (FLNC) MANE Select ENSP00000327145.8:n.*71C>A
ENST00000325888.12:c.*71C>A (FLNC) ENSP00000327145.8:n.*71C>A
ENST00000346177.6:c.*71C>A (FLNC) ENSP00000344002.6:n.*71C>A
NM_001127487.1:c.*71C>A (FLNC) NP_001120959.1:n.*71C>A
NM_001458.4:c.*71C>A , LRG_870t1:c.*71C>A (FLNC) NP_001449.3:n.*71C>A
NR_149055.1:n.102+3931G>T (FLNC-AS1)
NM_001127487.2:c.*71C>A (FLNC) NP_001120959.1:n.*71C>A
NM_001458.5:c.*71C>A (FLNC) MANE Select NP_001449.3:n.*71C>A