Canonical Allele Identifier: CA369220550
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128858164-C-A
MyVariant Identifiers: chr7:g.128498218C>A (hg19) chr7:g.128858164C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858164C>A , CM000669.2:g.128858164C>A GRCh38
NC_000007.13:g.128498218C>A , CM000669.1:g.128498218C>A GRCh37
NC_000007.12:g.128285454C>A NCBI36
NG_011807.1:g.32736C>A , LRG_870:g.32736C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7937C>A (FLNC) MANE Select ENSP00000327145.8:p.Ser2646Tyr
ENST00000325888.12:c.7937C>A (FLNC) ENSP00000327145.8:p.Ser2646Tyr
ENST00000346177.6:c.7838C>A (FLNC) ENSP00000344002.6:p.Ser2613Tyr
NM_001127487.1:c.7838C>A (FLNC) NP_001120959.1:p.Ser2613Tyr
NM_001458.4:c.7937C>A , LRG_870t1:c.7937C>A (FLNC) NP_001449.3:p.Ser2646Tyr
NR_149055.1:n.102+4361G>T (FLNC-AS1)
NM_001127487.2:c.7838C>A (FLNC) NP_001120959.1:p.Ser2613Tyr
NM_001458.5:c.7937C>A (FLNC) MANE Select NP_001449.3:p.Ser2646Tyr
Search 100 bp 5'
Search 100 bp 3'