Canonical Allele Identifier: CA1367512389

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58135848_58135850delinsCTA , CM000665.2:g.58135848_58135850delinsCTA	GRCh38
NC_000003.11:g.58121575_58121577delinsCTA , CM000665.1:g.58121575_58121577delinsCTA	GRCh37
NC_000003.10:g.58096615_58096617delinsCTA	NCBI36
NG_012801.1:g.132449_132451delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.96-131_96-129delinsCTA
ENST00000682868.1:n.6714-131_6714-129delinsCTA
ENST00000682871.1:c.4765-131_4765-129delinsCTA	ENSP00000507805.1:n.4765-131_4765-129delinsCTA
ENST00000684506.1:c.*3297-131_*3297-129delinsCTA	ENSP00000507728.1:n.*3297-131_*3297-129delinsCTA
ENST00000684607.1:c.4765-131_4765-129delinsCTA	ENSP00000508224.1:n.4765-131_4765-129delinsCTA
ENST00000295956.9:c.4672-131_4672-129delinsCTA MANE Select	ENSP00000295956.5:n.4672-131_4672-129delinsCTA
ENST00000295956.8:c.4672-131_4672-129delinsCTA	ENSP00000295956.4:n.4672-131_4672-129delinsCTA
ENST00000358537.7:c.4672-131_4672-129delinsCTA	ENSP00000351339.3:n.4672-131_4672-129delinsCTA
ENST00000429972.6:c.4672-131_4672-129delinsCTA	ENSP00000415599.2:n.4672-131_4672-129delinsCTA
ENST00000481470.5:n.1012-131_1012-129delinsCTA
ENST00000490882.5:c.4765-131_4765-129delinsCTA	ENSP00000420213.1:n.4765-131_4765-129delinsCTA
ENST00000493452.5:c.4165-131_4165-129delinsCTA	ENSP00000418510.1:n.4165-131_4165-129delinsCTA
NM_001164317.1:c.4765-131_4765-129delinsCTA	NP_001157789.1:n.4765-131_4765-129delinsCTA
NM_001164318.1:c.4672-131_4672-129delinsCTA	NP_001157790.1:n.4672-131_4672-129delinsCTA
NM_001164319.1:c.4672-131_4672-129delinsCTA	NP_001157791.1:n.4672-131_4672-129delinsCTA
NM_001457.3:c.4672-131_4672-129delinsCTA	NP_001448.2:n.4672-131_4672-129delinsCTA
XM_005264977.1:c.4765-131_4765-129delinsCTA	XP_005265034.1:n.4765-131_4765-129delinsCTA
XM_005264978.1:c.4765-131_4765-129delinsCTA	XP_005265035.1:n.4765-131_4765-129delinsCTA
XM_005264981.1:c.4765-131_4765-129delinsCTA	XP_005265038.1:n.4765-131_4765-129delinsCTA
XR_940396.1:n.4910-131_4910-129delinsCTA
XM_005264978.2:c.4765-131_4765-129delinsCTA	XP_005265035.1:n.4765-131_4765-129delinsCTA
XR_001740065.1:n.4910-131_4910-129delinsCTA
XR_940396.2:n.4910-131_4910-129delinsCTA
NM_001164317.2:c.4765-131_4765-129delinsCTA	NP_001157789.1:n.4765-131_4765-129delinsCTA
NM_001164318.2:c.4672-131_4672-129delinsCTA	NP_001157790.1:n.4672-131_4672-129delinsCTA
NM_001164319.2:c.4672-131_4672-129delinsCTA	NP_001157791.1:n.4672-131_4672-129delinsCTA
NM_001457.4:c.4672-131_4672-129delinsCTA MANE Select	NP_001448.2:n.4672-131_4672-129delinsCTA