Canonical Allele Identifier: CA369208132
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128851503-G-A
MyVariant Identifiers: chr7:g.128491557G>A (hg19) chr7:g.128851503G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851503G>A , CM000669.2:g.128851503G>A GRCh38
NC_000007.13:g.128491557G>A , CM000669.1:g.128491557G>A GRCh37
NC_000007.12:g.128278793G>A NCBI36
NG_011807.1:g.26075G>A , LRG_870:g.26075G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5717G>A (FLNC) MANE Select ENSP00000327145.8:p.Cys1906Tyr
ENST00000325888.12:c.5717G>A (FLNC) ENSP00000327145.8:p.Cys1906Tyr
ENST00000346177.6:c.5618G>A (FLNC) ENSP00000344002.6:p.Cys1873Tyr
NM_001127487.1:c.5618G>A (FLNC) NP_001120959.1:p.Cys1873Tyr
NM_001458.4:c.5717G>A , LRG_870t1:c.5717G>A (FLNC) NP_001449.3:p.Cys1906Tyr
NR_149055.1:n.216-3C>T (FLNC-AS1)
NM_001127487.2:c.5618G>A (FLNC) NP_001120959.1:p.Cys1873Tyr
NM_001458.5:c.5717G>A (FLNC) MANE Select NP_001449.3:p.Cys1906Tyr
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