Canonical Allele Identifier: CA1742516723
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128834972_128834975delinsCAGT , CM000669.2:g.128834972_128834975delinsCAGT GRCh38
NC_000007.13:g.128475026_128475029delinsCAGT , CM000669.1:g.128475026_128475029delinsCAGT GRCh37
NC_000007.12:g.128262262_128262265delinsCAGT NCBI36
NG_011807.1:g.9544_9547delinsCAGT , LRG_870:g.9544_9547delinsCAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-354_353-351delinsCAGT MANE Select ENSP00000327145.8:n.353-354_353-351delinsCAGT
ENST00000325888.12:c.353-354_353-351delinsCAGT ENSP00000327145.8:n.353-354_353-351delinsCAGT
ENST00000346177.6:c.353-354_353-351delinsCAGT ENSP00000344002.6:n.353-354_353-351delinsCAGT
NM_001127487.1:c.353-354_353-351delinsCAGT NP_001120959.1:n.353-354_353-351delinsCAGT
NM_001458.4:c.353-354_353-351delinsCAGT , LRG_870t1:c.353-354_353-351delinsCAGT NP_001449.3:n.353-354_353-351delinsCAGT
NM_001127487.2:c.353-354_353-351delinsCAGT NP_001120959.1:n.353-354_353-351delinsCAGT
NM_001458.5:c.353-354_353-351delinsCAGT MANE Select NP_001449.3:n.353-354_353-351delinsCAGT