Canonical Allele Identifier: CA369211433
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

COSMIC: COSM311224
MyVariant Identifiers: chr7:g.128493026G>T (hg19) chr7:g.128852972G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852972G>T , CM000669.2:g.128852972G>T GRCh38
NC_000007.13:g.128493026G>T , CM000669.1:g.128493026G>T GRCh37
NC_000007.12:g.128280262G>T NCBI36
NG_011807.1:g.27544G>T , LRG_870:g.27544G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6149G>T (FLNC) MANE Select ENSP00000327145.8:p.Gly2050Val
ENST00000325888.12:c.6149G>T (FLNC) ENSP00000327145.8:p.Gly2050Val
ENST00000346177.6:c.6050G>T (FLNC) ENSP00000344002.6:p.Gly2017Val
NM_001127487.1:c.6050G>T (FLNC) NP_001120959.1:p.Gly2017Val
NM_001458.4:c.6149G>T , LRG_870t1:c.6149G>T (FLNC) NP_001449.3:p.Gly2050Val
NR_149055.1:n.215+313C>A (FLNC-AS1)
NM_001127487.2:c.6050G>T (FLNC) NP_001120959.1:p.Gly2017Val
NM_001458.5:c.6149G>T (FLNC) MANE Select NP_001449.3:p.Gly2050Val
Search 100 bp 5'
Search 100 bp 3'