Canonical Allele Identifier: CA369221248
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1196459227
gnomAD v2: 7-128498427-G-C
gnomAD v4: 7-128858373-G-C
MyVariant Identifiers: chr7:g.128498427G>C (hg19) chr7:g.128858373G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858373G>C , CM000669.2:g.128858373G>C GRCh38
NC_000007.13:g.128498427G>C , CM000669.1:g.128498427G>C GRCh37
NC_000007.12:g.128285663G>C NCBI36
NG_011807.1:g.32945G>C , LRG_870:g.32945G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.8028G>C (FLNC) MANE Select ENSP00000327145.8:p.Lys2676Asn
ENST00000325888.12:c.8028G>C (FLNC) ENSP00000327145.8:p.Lys2676Asn
ENST00000346177.6:c.7929G>C (FLNC) ENSP00000344002.6:p.Lys2643Asn
NM_001127487.1:c.7929G>C (FLNC) NP_001120959.1:p.Lys2643Asn
NM_001458.4:c.8028G>C , LRG_870t1:c.8028G>C (FLNC) NP_001449.3:p.Lys2676Asn
NR_149055.1:n.102+4152C>G (FLNC-AS1)
NM_001127487.2:c.7929G>C (FLNC) NP_001120959.1:p.Lys2643Asn
NM_001458.5:c.8028G>C (FLNC) MANE Select NP_001449.3:p.Lys2676Asn
Search 100 bp 5'
Search 100 bp 3'