Canonical Allele Identifier: CA2684820168
Gene: FLNC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128839943_128839945del , CM000669.2:g.128839943_128839945del GRCh38
NC_000007.13:g.128479997_128479999del , CM000669.1:g.128479997_128479999del GRCh37
NC_000007.12:g.128267233_128267235del NCBI36
NG_011807.1:g.14515_14517del , LRG_870:g.14515_14517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1412-80_1412-78del MANE Select ENSP00000327145.8:n.1412-80_1412-78del
ENST00000325888.12:c.1412-80_1412-78del ENSP00000327145.8:n.1412-80_1412-78del
ENST00000346177.6:c.1412-80_1412-78del ENSP00000344002.6:n.1412-80_1412-78del
NM_001127487.1:c.1412-80_1412-78del NP_001120959.1:n.1412-80_1412-78del
NM_001458.4:c.1412-80_1412-78del , LRG_870t1:c.1412-80_1412-78del NP_001449.3:n.1412-80_1412-78del
NM_001127487.2:c.1412-80_1412-78del NP_001120959.1:n.1412-80_1412-78del
NM_001458.5:c.1412-80_1412-78del MANE Select NP_001449.3:n.1412-80_1412-78del