Canonical Allele Identifier: CA1742577408
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842760_128842761delinsAG , CM000669.2:g.128842760_128842761delinsAG GRCh38
NC_000007.13:g.128482814_128482815delinsAG , CM000669.1:g.128482814_128482815delinsAG GRCh37
NC_000007.12:g.128270050_128270051delinsAG NCBI36
NG_011807.1:g.17332_17333delinsAG , LRG_870:g.17332_17333delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2390-34_2390-33delinsAG MANE Select ENSP00000327145.8:n.2390-34_2390-33delins...
ENST00000325888.12:c.2390-34_2390-33delinsAG ENSP00000327145.8:n.2390-34_2390-33delins...
ENST00000346177.6:c.2390-34_2390-33delinsAG ENSP00000344002.6:n.2390-34_2390-33delins...
ENST00000388853.3:n.506-34_506-33delinsAG
NM_001127487.1:c.2390-34_2390-33delinsAG NP_001120959.1:n.2390-34_2390-33delinsAG
NM_001458.4:c.2390-34_2390-33delinsAG , LRG_870t1:c.2390-34_2390-33delinsAG NP_001449.3:n.2390-34_2390-33delinsAG
NM_001127487.2:c.2390-34_2390-33delinsAG NP_001120959.1:n.2390-34_2390-33delinsAG
NM_001458.5:c.2390-34_2390-33delinsAG MANE Select NP_001449.3:n.2390-34_2390-33delinsAG