Canonical Allele Identifier: CA457584240
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808868686
MyVariant Identifiers: chr7:g.128492703G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852649G>T , CM000669.2:g.128852649G>T GRCh38
NC_000007.13:g.128492703G>T , CM000669.1:g.128492703G>T GRCh37
NC_000007.12:g.128279939G>T NCBI36
NG_011807.1:g.27221G>T , LRG_870:g.27221G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5901G>T (FLNC) MANE Select ENSP00000327145.8:p.Leu1967=
ENST00000325888.12:c.5901G>T (FLNC) ENSP00000327145.8:p.Leu1967=
ENST00000346177.6:c.5802G>T (FLNC) ENSP00000344002.6:p.Leu1934=
NM_001127487.1:c.5802G>T (FLNC) NP_001120959.1:p.Leu1934=
NM_001458.4:c.5901G>T , LRG_870t1:c.5901G>T (FLNC) NP_001449.3:p.Leu1967=
NR_149055.1:n.215+636C>A (FLNC-AS1)
NM_001127487.2:c.5802G>T (FLNC) NP_001120959.1:p.Leu1934=
NM_001458.5:c.5901G>T (FLNC) MANE Select NP_001449.3:p.Leu1967=
Search 100 bp 5'
Search 100 bp 3'