Canonical Allele Identifier: CA1742516670
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128834929_128834930delinsTC , CM000669.2:g.128834929_128834930delinsTC GRCh38
NC_000007.13:g.128474983_128474984delinsTC , CM000669.1:g.128474983_128474984delinsTC GRCh37
NC_000007.12:g.128262219_128262220delinsTC NCBI36
NG_011807.1:g.9501_9502delinsTC , LRG_870:g.9501_9502delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.353-397_353-396delinsTC MANE Select ENSP00000327145.8:n.353-397_353-396delinsTC
ENST00000325888.12:c.353-397_353-396delinsTC ENSP00000327145.8:n.353-397_353-396delinsTC
ENST00000346177.6:c.353-397_353-396delinsTC ENSP00000344002.6:n.353-397_353-396delinsTC
NM_001127487.1:c.353-397_353-396delinsTC NP_001120959.1:n.353-397_353-396delinsTC
NM_001458.4:c.353-397_353-396delinsTC , LRG_870t1:c.353-397_353-396delinsTC NP_001449.3:n.353-397_353-396delinsTC
NM_001127487.2:c.353-397_353-396delinsTC NP_001120959.1:n.353-397_353-396delinsTC
NM_001458.5:c.353-397_353-396delinsTC MANE Select NP_001449.3:n.353-397_353-396delinsTC