Canonical Allele Identifier: CA353355149

Gene: FLNB

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58146961T>A , CM000665.2:g.58146961T>A	GRCh38
NC_000003.11:g.58132688T>A , CM000665.1:g.58132688T>A	GRCh37
NC_000003.10:g.58107728T>A	NCBI36
NG_012801.1:g.143562T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.1048T>A
ENST00000682871.1:c.5576T>A	ENSP00000507805.1:p.Ile1859Asn
ENST00000683925.1:n.1794T>A
ENST00000684439.1:n.2007T>A
ENST00000684506.1:c.*4249T>A	ENSP00000507728.1:n.*4249T>A
ENST00000684607.1:c.5717T>A	ENSP00000508224.1:p.Ile1906Asn
ENST00000295956.9:c.5696T>A MANE Select	ENSP00000295956.5:p.Ile1899Asn
ENST00000295956.8:c.5696T>A	ENSP00000295956.4:p.Ile1899Asn
ENST00000358537.7:c.5624T>A	ENSP00000351339.3:p.Ile1875Asn
ENST00000429972.6:c.5663T>A	ENSP00000415599.2:p.Ile1888Asn
ENST00000481470.5:n.1964T>A
ENST00000490882.5:c.5789T>A	ENSP00000420213.1:p.Ile1930Asn
ENST00000491408.1:n.284T>A
ENST00000493452.5:c.5117T>A	ENSP00000418510.1:p.Ile1706Asn
NM_001164317.1:c.5789T>A	NP_001157789.1:p.Ile1930Asn
NM_001164318.1:c.5663T>A	NP_001157790.1:p.Ile1888Asn
NM_001164319.1:c.5624T>A	NP_001157791.1:p.Ile1875Asn
NM_001457.3:c.5696T>A	NP_001448.2:p.Ile1899Asn
XM_005264977.1:c.5756T>A	XP_005265034.1:p.Ile1919Asn
XM_005264978.1:c.5717T>A	XP_005265035.1:p.Ile1906Asn
XM_005264981.1:c.5789T>A	XP_005265038.1:p.Ile1930Asn
XR_940396.1:n.5934T>A
XM_005264978.2:c.5717T>A	XP_005265035.1:p.Ile1906Asn
XR_001740065.1:n.5934T>A
XR_940396.2:n.5934T>A
NM_001164317.2:c.5789T>A	NP_001157789.1:p.Ile1930Asn
NM_001164318.2:c.5663T>A	NP_001157790.1:p.Ile1888Asn
NM_001164319.2:c.5624T>A	NP_001157791.1:p.Ile1875Asn
NM_001457.4:c.5696T>A MANE Select	NP_001448.2:p.Ile1899Asn