Canonical Allele Identifier: CA1742567369
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841075A= , CM000669.2:g.128841075A= GRCh38
NC_000007.13:g.128481129A= , CM000669.1:g.128481129A= GRCh37
NC_000007.12:g.128268365A= NCBI36
NG_011807.1:g.15647A= , LRG_870:g.15647A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1814-95A= MANE Select ENSP00000327145.8:n.1814-95A=
ENST00000325888.12:c.1814-95A= ENSP00000327145.8:n.1814-95A=
ENST00000346177.6:c.1814-95A= ENSP00000344002.6:n.1814-95A=
NM_001127487.1:c.1814-95A= NP_001120959.1:n.1814-95A=
NM_001458.4:c.1814-95A= , LRG_870t1:c.1814-95A= NP_001449.3:n.1814-95A=
NM_001127487.2:c.1814-95A= NP_001120959.1:n.1814-95A=
NM_001458.5:c.1814-95A= MANE Select NP_001449.3:n.1814-95A=
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