Canonical Allele Identifier: CA2684820211
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856676T>C , CM000669.2:g.128856676T>C GRCh38
NC_000007.13:g.128496730T>C , CM000669.1:g.128496730T>C GRCh37
NC_000007.12:g.128283966T>C NCBI36
NG_011807.1:g.31248T>C , LRG_870:g.31248T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7384+26T>C (FLNC) MANE Select ENSP00000327145.8:n.7384+26T>C
ENST00000325888.12:c.7384+26T>C (FLNC) ENSP00000327145.8:n.7384+26T>C
ENST00000346177.6:c.7285+26T>C (FLNC) ENSP00000344002.6:n.7285+26T>C
NM_001127487.1:c.7285+26T>C (FLNC) NP_001120959.1:n.7285+26T>C
NM_001458.4:c.7384+26T>C , LRG_870t1:c.7384+26T>C (FLNC) NP_001449.3:n.7384+26T>C
NR_149055.1:n.103-3279A>G (FLNC-AS1)
NM_001127487.2:c.7285+26T>C (FLNC) NP_001120959.1:n.7285+26T>C
NM_001458.5:c.7384+26T>C (FLNC) MANE Select NP_001449.3:n.7384+26T>C