Canonical Allele Identifier: CA2586972554

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58136032_58136043del , CM000665.2:g.58136032_58136043del	GRCh38
NC_000003.11:g.58121759_58121770del , CM000665.1:g.58121759_58121770del	GRCh37
NC_000003.10:g.58096799_58096810del	NCBI36
NG_012801.1:g.132633_132644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.149_160del
ENST00000682868.1:n.6767_6778del
ENST00000682871.1:c.4818_4829del	ENSP00000507805.1:p.Tyr1607_Thr1610del
ENST00000684506.1:c.*3350_*3361del	ENSP00000507728.1:n.*3350_*3361del
ENST00000684607.1:c.4818_4829del	ENSP00000508224.1:p.Tyr1607_Thr1610del
ENST00000295956.9:c.4725_4736del MANE Select	ENSP00000295956.5:p.Tyr1576_Thr1579del
ENST00000295956.8:c.4725_4736del	ENSP00000295956.4:p.Tyr1576_Thr1579del
ENST00000358537.7:c.4725_4736del	ENSP00000351339.3:p.Tyr1576_Thr1579del
ENST00000429972.6:c.4725_4736del	ENSP00000415599.2:p.Tyr1576_Thr1579del
ENST00000481470.5:n.1065_1076del
ENST00000490882.5:c.4818_4829del	ENSP00000420213.1:p.Tyr1607_Thr1610del
ENST00000493452.5:c.4218_4229del	ENSP00000418510.1:p.Tyr1407_Thr1410del
NM_001164317.1:c.4818_4829del	NP_001157789.1:p.Tyr1607_Thr1610del
NM_001164318.1:c.4725_4736del	NP_001157790.1:p.Tyr1576_Thr1579del
NM_001164319.1:c.4725_4736del	NP_001157791.1:p.Tyr1576_Thr1579del
NM_001457.3:c.4725_4736del	NP_001448.2:p.Tyr1576_Thr1579del
XM_005264977.1:c.4818_4829del	XP_005265034.1:p.Tyr1607_Thr1610del
XM_005264978.1:c.4818_4829del	XP_005265035.1:p.Tyr1607_Thr1610del
XM_005264981.1:c.4818_4829del	XP_005265038.1:p.Tyr1607_Thr1610del
XR_940396.1:n.4963_4974del
XM_005264978.2:c.4818_4829del	XP_005265035.1:p.Tyr1607_Thr1610del
XR_001740065.1:n.4963_4974del
XR_940396.2:n.4963_4974del
NM_001164317.2:c.4818_4829del	NP_001157789.1:p.Tyr1607_Thr1610del
NM_001164318.2:c.4725_4736del	NP_001157790.1:p.Tyr1576_Thr1579del
NM_001164319.2:c.4725_4736del	NP_001157791.1:p.Tyr1576_Thr1579del
NM_001457.4:c.4725_4736del MANE Select	NP_001448.2:p.Tyr1576_Thr1579del