Canonical Allele Identifier: CA1367486657

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58078724C= , CM000665.2:g.58078724C=	GRCh38
NC_000003.11:g.58064451C= , CM000665.1:g.58064451C=	GRCh37
NC_000003.10:g.58039491C=	NCBI36
NG_012801.1:g.75325C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682097.1:c.549C=	ENSP00000508183.1:p.Cys183=
ENST00000682868.1:n.692C=
ENST00000682871.1:c.549C=	ENSP00000507805.1:p.Cys183=
ENST00000682987.1:n.692C=
ENST00000683511.1:n.708C=
ENST00000684107.1:c.549C=	ENSP00000507440.1:p.Cys183=
ENST00000684506.1:c.549C=	ENSP00000507728.1:p.Cys183=
ENST00000684517.1:c.549C=	ENSP00000507828.1:p.Cys183=
ENST00000684607.1:c.549C=	ENSP00000508224.1:p.Cys183=
ENST00000295956.9:c.549C= MANE Select	ENSP00000295956.5:p.Cys183=
ENST00000295956.8:c.549C=	ENSP00000295956.4:p.Cys183=
ENST00000358537.7:c.549C=	ENSP00000351339.3:p.Cys183=
ENST00000429972.6:c.549C=	ENSP00000415599.2:p.Cys183=
ENST00000490882.5:c.549C=	ENSP00000420213.1:p.Cys183=
ENST00000493452.5:c.42C=	ENSP00000418510.1:p.Cys14=
NM_001164317.1:c.549C=	NP_001157789.1:p.Cys183=
NM_001164318.1:c.549C=	NP_001157790.1:p.Cys183=
NM_001164319.1:c.549C=	NP_001157791.1:p.Cys183=
NM_001457.3:c.549C=	NP_001448.2:p.Cys183=
XM_005264977.1:c.549C=	XP_005265034.1:p.Cys183=
XM_005264978.1:c.549C=	XP_005265035.1:p.Cys183=
XM_005264981.1:c.549C=	XP_005265038.1:p.Cys183=
XR_940396.1:n.694C=
XM_005264978.2:c.549C=	XP_005265035.1:p.Cys183=
XR_001740065.1:n.694C=
XR_940396.2:n.694C=
NM_001164317.2:c.549C=	NP_001157789.1:p.Cys183=
NM_001164318.2:c.549C=	NP_001157790.1:p.Cys183=
NM_001164319.2:c.549C=	NP_001157791.1:p.Cys183=
NM_001457.4:c.549C= MANE Select	NP_001448.2:p.Cys183=