Canonical Allele Identifier: CA1367516837

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58145997A= , CM000665.2:g.58145997A=	GRCh38
NC_000003.11:g.58131724A= , CM000665.1:g.58131724A=	GRCh37
NC_000003.10:g.58106764A=	NCBI36
NG_012801.1:g.142598A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682297.1:n.854A=
ENST00000682871.1:c.5382A=	ENSP00000507805.1:p.Gly1794=
ENST00000683925.1:n.1600A=
ENST00000684439.1:n.1813A=
ENST00000684506.1:c.*4055A=	ENSP00000507728.1:n.*4055A=
ENST00000684607.1:c.5523A=	ENSP00000508224.1:p.Gly1841=
ENST00000295956.9:c.5502A= MANE Select	ENSP00000295956.5:p.Gly1834=
ENST00000295956.8:c.5502A=	ENSP00000295956.4:p.Gly1834=
ENST00000358537.7:c.5430A=	ENSP00000351339.3:p.Gly1810=
ENST00000429972.6:c.5469A=	ENSP00000415599.2:p.Gly1823=
ENST00000481470.5:n.1770A=
ENST00000490882.5:c.5595A=	ENSP00000420213.1:p.Gly1865=
ENST00000493452.5:c.4923A=	ENSP00000418510.1:p.Gly1641=
NM_001164317.1:c.5595A=	NP_001157789.1:p.Gly1865=
NM_001164318.1:c.5469A=	NP_001157790.1:p.Gly1823=
NM_001164319.1:c.5430A=	NP_001157791.1:p.Gly1810=
NM_001457.3:c.5502A=	NP_001448.2:p.Gly1834=
XM_005264977.1:c.5562A=	XP_005265034.1:p.Gly1854=
XM_005264978.1:c.5523A=	XP_005265035.1:p.Gly1841=
XM_005264981.1:c.5595A=	XP_005265038.1:p.Gly1865=
XR_940396.1:n.5740A=
XM_005264978.2:c.5523A=	XP_005265035.1:p.Gly1841=
XR_001740065.1:n.5740A=
XR_940396.2:n.5740A=
NM_001164317.2:c.5595A=	NP_001157789.1:p.Gly1865=
NM_001164318.2:c.5469A=	NP_001157790.1:p.Gly1823=
NM_001164319.2:c.5430A=	NP_001157791.1:p.Gly1810=
NM_001457.4:c.5502A= MANE Select	NP_001448.2:p.Gly1834=