Canonical Allele Identifier: CA1742574277
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808862803
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852542A>T , CM000669.2:g.128852542A>T GRCh38
NC_000007.13:g.128492596A>T , CM000669.1:g.128492596A>T GRCh37
NC_000007.12:g.128279832A>T NCBI36
NG_011807.1:g.27114A>T , LRG_870:g.27114A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5843-49A>T (FLNC) MANE Select ENSP00000327145.8:n.5843-49A>T
ENST00000325888.12:c.5843-49A>T (FLNC) ENSP00000327145.8:n.5843-49A>T
ENST00000346177.6:c.5744-49A>T (FLNC) ENSP00000344002.6:n.5744-49A>T
NM_001127487.1:c.5744-49A>T (FLNC) NP_001120959.1:n.5744-49A>T
NM_001458.4:c.5843-49A>T , LRG_870t1:c.5843-49A>T (FLNC) NP_001449.3:n.5843-49A>T
NR_149055.1:n.215+743T>A (FLNC-AS1)
NM_001127487.2:c.5744-49A>T (FLNC) NP_001120959.1:n.5744-49A>T
NM_001458.5:c.5843-49A>T (FLNC) MANE Select NP_001449.3:n.5843-49A>T
Search 100 bp 5'
Search 100 bp 3'