Canonical Allele Identifier: CA369213659
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs751019991
gnomAD v3: 7-128854464-A-C
gnomAD v4: 7-128854464-A-C
MyVariant Identifiers: chr7:g.128494518A>C (hg19) chr7:g.128854464A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854464A>C , CM000669.2:g.128854464A>C GRCh38
NC_000007.13:g.128494518A>C , CM000669.1:g.128494518A>C GRCh37
NC_000007.12:g.128281754A>C NCBI36
NG_011807.1:g.29036A>C , LRG_870:g.29036A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6779A>C (FLNC) MANE Select ENSP00000327145.8:p.Lys2260Thr
ENST00000325888.12:c.6779A>C (FLNC) ENSP00000327145.8:p.Lys2260Thr
ENST00000346177.6:c.6680A>C (FLNC) ENSP00000344002.6:p.Lys2227Thr
NM_001127487.1:c.6680A>C (FLNC) NP_001120959.1:p.Lys2227Thr
NM_001458.4:c.6779A>C , LRG_870t1:c.6779A>C (FLNC) NP_001449.3:p.Lys2260Thr
NR_149055.1:n.103-1067T>G (FLNC-AS1)
NM_001127487.2:c.6680A>C (FLNC) NP_001120959.1:p.Lys2227Thr
NM_001458.5:c.6779A>C (FLNC) MANE Select NP_001449.3:p.Lys2260Thr
Search 100 bp 5'
Search 100 bp 3'