Canonical Allele Identifier: CA1742563706
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849197_128849198delinsTG , CM000669.2:g.128849197_128849198delinsTG GRCh38
NC_000007.13:g.128489251_128489252delinsTG , CM000669.1:g.128489251_128489252delinsTG GRCh37
NC_000007.12:g.128276487_128276488delinsTG NCBI36
NG_011807.1:g.23769_23770delinsTG , LRG_870:g.23769_23770delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4944_4945delinsTG MANE Select ENSP00000327145.8:p.His1648=
ENST00000325888.12:c.4944_4945delinsTG ENSP00000327145.8:p.His1648=
ENST00000346177.6:c.4944_4945delinsTG ENSP00000344002.6:p.His1648=
NM_001127487.1:c.4944_4945delinsTG NP_001120959.1:p.His1648=
NM_001458.4:c.4944_4945delinsTG , LRG_870t1:c.4944_4945delinsTG NP_001449.3:p.His1648=
NM_001127487.2:c.4944_4945delinsTG NP_001120959.1:p.His1648=
NM_001458.5:c.4944_4945delinsTG MANE Select NP_001449.3:p.His1648=