Canonical Allele Identifier: CA1367495335

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58097741G= , CM000665.2:g.58097741G=	GRCh38
NC_000003.11:g.58083468G= , CM000665.1:g.58083468G=	GRCh37
NC_000003.10:g.58058508G=	NCBI36
NG_012801.1:g.94342G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682097.1:c.985-74G=	ENSP00000508183.1:n.985-74G=
ENST00000682868.1:n.1128-74G=
ENST00000682871.1:c.985-74G=	ENSP00000507805.1:n.985-74G=
ENST00000682987.1:n.1128-74G=
ENST00000683511.1:n.1144-74G=
ENST00000684107.1:c.985-74G=	ENSP00000507440.1:n.985-74G=
ENST00000684506.1:c.985-74G=	ENSP00000507728.1:n.985-74G=
ENST00000684517.1:c.985-74G=	ENSP00000507828.1:n.985-74G=
ENST00000684607.1:c.985-74G=	ENSP00000508224.1:n.985-74G=
ENST00000295956.9:c.985-74G= MANE Select	ENSP00000295956.5:n.985-74G=
ENST00000295956.8:c.985-74G=	ENSP00000295956.4:n.985-74G=
ENST00000358537.7:c.985-74G=	ENSP00000351339.3:n.985-74G=
ENST00000429972.6:c.985-74G=	ENSP00000415599.2:n.985-74G=
ENST00000490882.5:c.985-74G=	ENSP00000420213.1:n.985-74G=
ENST00000493452.5:c.478-74G=	ENSP00000418510.1:n.478-74G=
NM_001164317.1:c.985-74G=	NP_001157789.1:n.985-74G=
NM_001164318.1:c.985-74G=	NP_001157790.1:n.985-74G=
NM_001164319.1:c.985-74G=	NP_001157791.1:n.985-74G=
NM_001457.3:c.985-74G=	NP_001448.2:n.985-74G=
XM_005264977.1:c.985-74G=	XP_005265034.1:n.985-74G=
XM_005264978.1:c.985-74G=	XP_005265035.1:n.985-74G=
XM_005264981.1:c.985-74G=	XP_005265038.1:n.985-74G=
XR_940396.1:n.1130-74G=
XM_005264978.2:c.985-74G=	XP_005265035.1:n.985-74G=
XR_001740065.1:n.1130-74G=
XR_940396.2:n.1130-74G=
NM_001164317.2:c.985-74G=	NP_001157789.1:n.985-74G=
NM_001164318.2:c.985-74G=	NP_001157790.1:n.985-74G=
NM_001164319.2:c.985-74G=	NP_001157791.1:n.985-74G=
NM_001457.4:c.985-74G= MANE Select	NP_001448.2:n.985-74G=