Canonical Allele Identifier: CA1742563753

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849216_128849220delinsTTCTC , CM000669.2:g.128849216_128849220delinsTTCTC	GRCh38
NC_000007.13:g.128489270_128489274delinsTTCTC , CM000669.1:g.128489270_128489274delinsTTCTC	GRCh37
NC_000007.12:g.128276506_128276510delinsTTCTC	NCBI36
NG_011807.1:g.23788_23792delinsTTCTC , LRG_870:g.23788_23792delinsTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4951+12_4951+16delinsTTCTC MANE Select	ENSP00000327145.8:n.4951+12_4951+16delinsTTCTC
ENST00000325888.12:c.4951+12_4951+16delinsTTCTC	ENSP00000327145.8:n.4951+12_4951+16delinsTTCTC
ENST00000346177.6:c.4951+12_4951+16delinsTTCTC	ENSP00000344002.6:n.4951+12_4951+16delinsTTCTC
NM_001127487.1:c.4951+12_4951+16delinsTTCTC	NP_001120959.1:n.4951+12_4951+16delinsTTCTC
NM_001458.4:c.4951+12_4951+16delinsTTCTC , LRG_870t1:c.4951+12_4951+16delinsTTCTC	NP_001449.3:n.4951+12_4951+16delinsTTCTC
NM_001127487.2:c.4951+12_4951+16delinsTTCTC	NP_001120959.1:n.4951+12_4951+16delinsTTCTC
NM_001458.5:c.4951+12_4951+16delinsTTCTC MANE Select	NP_001449.3:n.4951+12_4951+16delinsTTCTC