Canonical Allele Identifier: CA457849162
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128851501-C-T
MyVariant Identifiers: chr7:g.128491555C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851501C>T , CM000669.2:g.128851501C>T GRCh38
NC_000007.13:g.128491555C>T , CM000669.1:g.128491555C>T GRCh37
NC_000007.12:g.128278791C>T NCBI36
NG_011807.1:g.26073C>T , LRG_870:g.26073C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5715C>T (FLNC) MANE Select ENSP00000327145.8:p.Thr1905=
ENST00000325888.12:c.5715C>T (FLNC) ENSP00000327145.8:p.Thr1905=
ENST00000346177.6:c.5616C>T (FLNC) ENSP00000344002.6:p.Thr1872=
NM_001127487.1:c.5616C>T (FLNC) NP_001120959.1:p.Thr1872=
NM_001458.4:c.5715C>T , LRG_870t1:c.5715C>T (FLNC) NP_001449.3:p.Thr1905=
NR_149055.1:n.216-1G>A (FLNC-AS1)
NM_001127487.2:c.5616C>T (FLNC) NP_001120959.1:p.Thr1872=
NM_001458.5:c.5715C>T (FLNC) MANE Select NP_001449.3:p.Thr1905=
Search 100 bp 5'
Search 100 bp 3'