Canonical Allele Identifier: CA1367518053

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58148771C= , CM000665.2:g.58148771C=	GRCh38
NC_000003.11:g.58134498C= , CM000665.1:g.58134498C=	GRCh37
NC_000003.10:g.58109538C=	NCBI36
NG_012801.1:g.145372C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001457.4:c.6010C= MANE Select	NP_001448.2:p.Arg2004=
ENST00000295956.9:c.6010C= MANE Select	ENSP00000295956.5:p.Arg2004=
NM_001164317.1:c.6103C=	NP_001157789.1:p.Arg2035=
NM_001164317.2:c.6103C=	NP_001157789.1:p.Arg2035=
NM_001164318.1:c.5977C=	NP_001157790.1:p.Arg1993=
NM_001164318.2:c.5977C=	NP_001157790.1:p.Arg1993=
NM_001164319.1:c.5938C=	NP_001157791.1:p.Arg1980=
NM_001164319.2:c.5938C=	NP_001157791.1:p.Arg1980=
NM_001457.3:c.6010C=	NP_001448.2:p.Arg2004=
ENST00000295956.8:c.6010C=	ENSP00000295956.4:p.Arg2004=
ENST00000358537.7:c.5938C=	ENSP00000351339.3:p.Arg1980=
ENST00000429972.6:c.5977C=	ENSP00000415599.2:p.Arg1993=
ENST00000481470.5:n.2278C=
ENST00000490882.5:c.6103C=	ENSP00000420213.1:p.Arg2035=
ENST00000493452.5:c.5431C=	ENSP00000418510.1:p.Arg1811=
ENST00000682297.1:n.1362C=
ENST00000682871.1:c.5890C=	ENSP00000507805.1:p.Arg1964=
ENST00000683925.1:n.2108C=
ENST00000684439.1:n.2321C=
ENST00000684506.1:c.*4563C=	ENSP00000507728.1:n.*4563C=
ENST00000684607.1:c.6031C=	ENSP00000508224.1:p.Arg2011=
XM_005264977.1:c.6070C=	XP_005265034.1:p.Arg2024=
XM_005264978.1:c.6031C=	XP_005265035.1:p.Arg2011=
XM_005264978.2:c.6031C=	XP_005265035.1:p.Arg2011=
XM_005264981.1:c.6103C=	XP_005265038.1:p.Arg2035=
XR_001740065.1:n.6248C=
XR_940396.1:n.6248C=
XR_940396.2:n.6248C=