Canonical Allele Identifier: CA457849134
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128491540C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851486C>A , CM000669.2:g.128851486C>A GRCh38
NC_000007.13:g.128491540C>A , CM000669.1:g.128491540C>A GRCh37
NC_000007.12:g.128278776C>A NCBI36
NG_011807.1:g.26058C>A , LRG_870:g.26058C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5700C>A (FLNC) MANE Select ENSP00000327145.8:p.Ser1900=
ENST00000325888.12:c.5700C>A (FLNC) ENSP00000327145.8:p.Ser1900=
ENST00000346177.6:c.5601C>A (FLNC) ENSP00000344002.6:p.Ser1867=
NM_001127487.1:c.5601C>A (FLNC) NP_001120959.1:p.Ser1867=
NM_001458.4:c.5700C>A , LRG_870t1:c.5700C>A (FLNC) NP_001449.3:p.Ser1900=
NR_149055.1:n.230G>T (FLNC-AS1)
NM_001127487.2:c.5601C>A (FLNC) NP_001120959.1:p.Ser1867=
NM_001458.5:c.5700C>A (FLNC) MANE Select NP_001449.3:p.Ser1900=