Canonical Allele Identifier: CA2563311744

Gene: FLNC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849267_128849268insTTAAAAAAA , CM000669.2:g.128849267_128849268insTTAAAAAAA	GRCh38
NC_000007.13:g.128489321_128489322insTTAAAAAAA , CM000669.1:g.128489321_128489322insTTAAAAAAA	GRCh37
NC_000007.12:g.128276557_128276558insTTAAAAAAA	NCBI36
NG_011807.1:g.23839_23840insTTAAAAAAA , LRG_870:g.23839_23840insTTAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.4952-64_4952-63insTTAAAAAAA MANE Select	ENSP00000327145.8:n.4952-64_4952-63insTTAAAAAAA
ENST00000325888.12:c.4952-64_4952-63insTTAAAAAAA	ENSP00000327145.8:n.4952-64_4952-63insTTAAAAAAA
ENST00000346177.6:c.4952-64_4952-63insTTAAAAAAA	ENSP00000344002.6:n.4952-64_4952-63insTTAAAAAAA
NM_001127487.1:c.4952-64_4952-63insTTAAAAAAA	NP_001120959.1:n.4952-64_4952-63insTTAAAAAAA
NM_001458.4:c.4952-64_4952-63insTTAAAAAAA , LRG_870t1:c.4952-64_4952-63insTTAAAAAAA	NP_001449.3:n.4952-64_4952-63insTTAAAAAAA
NM_001127487.2:c.4952-64_4952-63insTTAAAAAAA	NP_001120959.1:n.4952-64_4952-63insTTAAAAAAA
NM_001458.5:c.4952-64_4952-63insTTAAAAAAA MANE Select	NP_001449.3:n.4952-64_4952-63insTTAAAAAAA