Canonical Allele Identifier: CA1367500644

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58109631T= , CM000665.2:g.58109631T=	GRCh38
NC_000003.11:g.58095358T= , CM000665.1:g.58095358T=	GRCh37
NC_000003.10:g.58070398T=	NCBI36
NG_012801.1:g.106232T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682868.1:n.2398T=
ENST00000682871.1:c.2255T=	ENSP00000507805.1:p.Val752=
ENST00000684107.1:c.*787T=	ENSP00000507440.1:n.*787T=
ENST00000684506.1:c.*787T=	ENSP00000507728.1:n.*787T=
ENST00000684517.1:c.*787T=	ENSP00000507828.1:n.*787T=
ENST00000684607.1:c.2255T=	ENSP00000508224.1:p.Val752=
ENST00000295956.9:c.2255T= MANE Select	ENSP00000295956.5:p.Val752=
ENST00000295956.8:c.2255T=	ENSP00000295956.4:p.Val752=
ENST00000358537.7:c.2255T=	ENSP00000351339.3:p.Val752=
ENST00000429972.6:c.2255T=	ENSP00000415599.2:p.Val752=
ENST00000490882.5:c.2255T=	ENSP00000420213.1:p.Val752=
ENST00000493452.5:c.1748T=	ENSP00000418510.1:p.Val583=
NM_001164317.1:c.2255T=	NP_001157789.1:p.Val752=
NM_001164318.1:c.2255T=	NP_001157790.1:p.Val752=
NM_001164319.1:c.2255T=	NP_001157791.1:p.Val752=
NM_001457.3:c.2255T=	NP_001448.2:p.Val752=
XM_005264977.1:c.2255T=	XP_005265034.1:p.Val752=
XM_005264978.1:c.2255T=	XP_005265035.1:p.Val752=
XM_005264981.1:c.2255T=	XP_005265038.1:p.Val752=
XR_940396.1:n.2400T=
XM_005264978.2:c.2255T=	XP_005265035.1:p.Val752=
XR_001740065.1:n.2400T=
XR_940396.2:n.2400T=
NM_001164317.2:c.2255T=	NP_001157789.1:p.Val752=
NM_001164318.2:c.2255T=	NP_001157790.1:p.Val752=
NM_001164319.2:c.2255T=	NP_001157791.1:p.Val752=
NM_001457.4:c.2255T= MANE Select	NP_001448.2:p.Val752=