Canonical Allele Identifier: CA908627946

Gene: FLNB

Linked Data

• dbSNP Id: rs1435536515
• gnomAD v3: 3-58136085-CCTACG-C
• gnomAD v4: 3-58136085-CCTACG-C
• MyVariant Identifiers: chr3:g.58121813_58121817del (hg19) ; chr3:g.58136086_58136090del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58136086_58136090del , CM000665.2:g.58136086_58136090del	GRCh38
NC_000003.11:g.58121813_58121817del , CM000665.1:g.58121813_58121817del	GRCh37
NC_000003.10:g.58096853_58096857del	NCBI36
NG_012801.1:g.132687_132691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.203_207del
ENST00000682868.1:n.6821_6825del
ENST00000682871.1:c.4872_4876del	ENSP00000507805.1:p.Tyr1625GlyfsTer2
ENST00000684506.1:c.*3404_*3408del	ENSP00000507728.1:n.*3404_*3408del
ENST00000684607.1:c.4872_4876del	ENSP00000508224.1:p.Tyr1625GlyfsTer2
ENST00000295956.9:c.4779_4783del MANE Select	ENSP00000295956.5:p.Tyr1594GlyfsTer2
ENST00000295956.8:c.4779_4783del	ENSP00000295956.4:p.Tyr1594GlyfsTer2
ENST00000358537.7:c.4779_4783del	ENSP00000351339.3:p.Tyr1594GlyfsTer2
ENST00000429972.6:c.4779_4783del	ENSP00000415599.2:p.Tyr1594GlyfsTer2
ENST00000481470.5:n.1119_1123del
ENST00000490882.5:c.4872_4876del	ENSP00000420213.1:p.Tyr1625GlyfsTer2
ENST00000493452.5:c.4272_4276del	ENSP00000418510.1:p.Tyr1425GlyfsTer2
NM_001164317.1:c.4872_4876del	NP_001157789.1:p.Tyr1625GlyfsTer2
NM_001164318.1:c.4779_4783del	NP_001157790.1:p.Tyr1594GlyfsTer2
NM_001164319.1:c.4779_4783del	NP_001157791.1:p.Tyr1594GlyfsTer2
NM_001457.3:c.4779_4783del	NP_001448.2:p.Tyr1594GlyfsTer2
XM_005264977.1:c.4872_4876del	XP_005265034.1:p.Tyr1625GlyfsTer2
XM_005264978.1:c.4872_4876del	XP_005265035.1:p.Tyr1625GlyfsTer2
XM_005264981.1:c.4872_4876del	XP_005265038.1:p.Tyr1625GlyfsTer2
XR_940396.1:n.5017_5021del
XM_005264978.2:c.4872_4876del	XP_005265035.1:p.Tyr1625GlyfsTer2
XR_001740065.1:n.5017_5021del
XR_940396.2:n.5017_5021del
NM_001164317.2:c.4872_4876del	NP_001157789.1:p.Tyr1625GlyfsTer2
NM_001164318.2:c.4779_4783del	NP_001157790.1:p.Tyr1594GlyfsTer2
NM_001164319.2:c.4779_4783del	NP_001157791.1:p.Tyr1594GlyfsTer2
NM_001457.4:c.4779_4783del MANE Select	NP_001448.2:p.Tyr1594GlyfsTer2