Canonical Allele Identifier: CA1742516688
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128834945G= , CM000669.2:g.128834945G= GRCh38
NC_000007.13:g.128474999G= , CM000669.1:g.128474999G= GRCh37
NC_000007.12:g.128262235G= NCBI36
NG_011807.1:g.9517G= , LRG_870:g.9517G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-381G= MANE Select ENSP00000327145.8:n.353-381G=
ENST00000325888.12:c.353-381G= ENSP00000327145.8:n.353-381G=
ENST00000346177.6:c.353-381G= ENSP00000344002.6:n.353-381G=
NM_001127487.1:c.353-381G= NP_001120959.1:n.353-381G=
NM_001458.4:c.353-381G= , LRG_870t1:c.353-381G= NP_001449.3:n.353-381G=
NM_001127487.2:c.353-381G= NP_001120959.1:n.353-381G=
NM_001458.5:c.353-381G= MANE Select NP_001449.3:n.353-381G=
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