Canonical Allele Identifier: CA457588876
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128495341T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128855287T>A , CM000669.2:g.128855287T>A GRCh38
NC_000007.13:g.128495341T>A , CM000669.1:g.128495341T>A GRCh37
NC_000007.12:g.128282577T>A NCBI36
NG_011807.1:g.29859T>A , LRG_870:g.29859T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7224T>A (FLNC) MANE Select ENSP00000327145.8:p.Ala2408=
ENST00000325888.12:c.7224T>A (FLNC) ENSP00000327145.8:p.Ala2408=
ENST00000346177.6:c.7125T>A (FLNC) ENSP00000344002.6:p.Ala2375=
NM_001127487.1:c.7125T>A (FLNC) NP_001120959.1:p.Ala2375=
NM_001458.4:c.7224T>A , LRG_870t1:c.7224T>A (FLNC) NP_001449.3:p.Ala2408=
NR_149055.1:n.103-1890A>T (FLNC-AS1)
NM_001127487.2:c.7125T>A (FLNC) NP_001120959.1:p.Ala2375=
NM_001458.5:c.7224T>A (FLNC) MANE Select NP_001449.3:p.Ala2408=