Canonical Allele Identifier: CA1742545965
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128840185G= , CM000669.2:g.128840185G= GRCh38
NC_000007.13:g.128480239G= , CM000669.1:g.128480239G= GRCh37
NC_000007.12:g.128267475G= NCBI36
NG_011807.1:g.14757G= , LRG_870:g.14757G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1549+25G= MANE Select ENSP00000327145.8:n.1549+25G=
ENST00000325888.12:c.1549+25G= ENSP00000327145.8:n.1549+25G=
ENST00000346177.6:c.1549+25G= ENSP00000344002.6:n.1549+25G=
NM_001127487.1:c.1549+25G= NP_001120959.1:n.1549+25G=
NM_001458.4:c.1549+25G= , LRG_870t1:c.1549+25G= NP_001449.3:n.1549+25G=
NM_001127487.2:c.1549+25G= NP_001120959.1:n.1549+25G=
NM_001458.5:c.1549+25G= MANE Select NP_001449.3:n.1549+25G=
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