Canonical Allele Identifier: CA1367512482

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58136082T= , CM000665.2:g.58136082T=	GRCh38
NC_000003.11:g.58121809T= , CM000665.1:g.58121809T=	GRCh37
NC_000003.10:g.58096849T=	NCBI36
NG_012801.1:g.132683T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.199T=
ENST00000682868.1:n.6817T=
ENST00000682871.1:c.4868T=	ENSP00000507805.1:p.Val1623=
ENST00000684506.1:c.*3400T=	ENSP00000507728.1:n.*3400T=
ENST00000684607.1:c.4868T=	ENSP00000508224.1:p.Val1623=
ENST00000295956.9:c.4775T= MANE Select	ENSP00000295956.5:p.Val1592=
ENST00000295956.8:c.4775T=	ENSP00000295956.4:p.Val1592=
ENST00000358537.7:c.4775T=	ENSP00000351339.3:p.Val1592=
ENST00000429972.6:c.4775T=	ENSP00000415599.2:p.Val1592=
ENST00000481470.5:n.1115T=
ENST00000490882.5:c.4868T=	ENSP00000420213.1:p.Val1623=
ENST00000493452.5:c.4268T=	ENSP00000418510.1:p.Val1423=
NM_001164317.1:c.4868T=	NP_001157789.1:p.Val1623=
NM_001164318.1:c.4775T=	NP_001157790.1:p.Val1592=
NM_001164319.1:c.4775T=	NP_001157791.1:p.Val1592=
NM_001457.3:c.4775T=	NP_001448.2:p.Val1592=
XM_005264977.1:c.4868T=	XP_005265034.1:p.Val1623=
XM_005264978.1:c.4868T=	XP_005265035.1:p.Val1623=
XM_005264981.1:c.4868T=	XP_005265038.1:p.Val1623=
XR_940396.1:n.5013T=
XM_005264978.2:c.4868T=	XP_005265035.1:p.Val1623=
XR_001740065.1:n.5013T=
XR_940396.2:n.5013T=
NM_001164317.2:c.4868T=	NP_001157789.1:p.Val1623=
NM_001164318.2:c.4775T=	NP_001157790.1:p.Val1592=
NM_001164319.2:c.4775T=	NP_001157791.1:p.Val1592=
NM_001457.4:c.4775T= MANE Select	NP_001448.2:p.Val1592=