Canonical Allele Identifier: CA1742584279
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128844877_128844878delinsGC , CM000669.2:g.128844877_128844878delinsGC GRCh38
NC_000007.13:g.128484931_128484932delinsGC , CM000669.1:g.128484931_128484932delinsGC GRCh37
NC_000007.12:g.128272167_128272168delinsGC NCBI36
NG_011807.1:g.19449_19450delinsGC , LRG_870:g.19449_19450delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3412_3413delinsGC MANE Select ENSP00000327145.8:p.Ala1138=
ENST00000325888.12:c.3412_3413delinsGC ENSP00000327145.8:p.Ala1138=
ENST00000346177.6:c.3412_3413delinsGC ENSP00000344002.6:p.Ala1138=
NM_001127487.1:c.3412_3413delinsGC NP_001120959.1:p.Ala1138=
NM_001458.4:c.3412_3413delinsGC , LRG_870t1:c.3412_3413delinsGC NP_001449.3:p.Ala1138=
NM_001127487.2:c.3412_3413delinsGC NP_001120959.1:p.Ala1138=
NM_001458.5:c.3412_3413delinsGC MANE Select NP_001449.3:p.Ala1138=
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