Canonical Allele Identifier: CA2840039198
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854232T>A , CM000669.2:g.128854232T>A GRCh38
NC_000007.13:g.128494286T>A , CM000669.1:g.128494286T>A GRCh37
NC_000007.12:g.128281522T>A NCBI36
NG_011807.1:g.28804T>A , LRG_870:g.28804T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6727+16T>A (FLNC) MANE Select ENSP00000327145.8:n.6727+16T>A
ENST00000325888.12:c.6727+16T>A (FLNC) ENSP00000327145.8:n.6727+16T>A
ENST00000346177.6:c.6628+16T>A (FLNC) ENSP00000344002.6:n.6628+16T>A
NM_001127487.1:c.6628+16T>A (FLNC) NP_001120959.1:n.6628+16T>A
NM_001458.4:c.6727+16T>A , LRG_870t1:c.6727+16T>A (FLNC) NP_001449.3:n.6727+16T>A
NR_149055.1:n.103-835A>T (FLNC-AS1)
NM_001127487.2:c.6628+16T>A (FLNC) NP_001120959.1:n.6628+16T>A
NM_001458.5:c.6727+16T>A (FLNC) MANE Select NP_001449.3:n.6727+16T>A