Canonical Allele Identifier: CA2469463

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58154840C>T , CM000665.2:g.58154840C>T	GRCh38
NC_000003.11:g.58140567C>T , CM000665.1:g.58140567C>T	GRCh37
NC_000003.10:g.58115607C>T	NCBI36
NG_012801.1:g.151441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.2036C>T
ENST00000682503.1:n.884C>T
ENST00000682871.1:c.6564C>T	ENSP00000507805.1:p.Ile2188=
ENST00000683114.1:n.1355C>T
ENST00000684439.1:n.2995C>T
ENST00000684506.1:c.*5237C>T	ENSP00000507728.1:n.*5237C>T
ENST00000684607.1:c.6705C>T	ENSP00000508224.1:p.Ile2235=
ENST00000295956.9:c.6684C>T MANE Select	ENSP00000295956.5:p.Ile2228=
ENST00000295956.8:c.6684C>T	ENSP00000295956.4:p.Ile2228=
ENST00000358537.7:c.6612C>T	ENSP00000351339.3:p.Ile2204=
ENST00000429972.6:c.6651C>T	ENSP00000415599.2:p.Ile2217=
ENST00000468939.1:n.231C>T
ENST00000481470.5:n.2952C>T
ENST00000490882.5:c.6777C>T	ENSP00000420213.1:p.Ile2259=
ENST00000493452.5:c.6105C>T	ENSP00000418510.1:p.Ile2035=
NM_001164317.1:c.6777C>T	NP_001157789.1:p.Ile2259=
NM_001164318.1:c.6651C>T	NP_001157790.1:p.Ile2217=
NM_001164319.1:c.6612C>T	NP_001157791.1:p.Ile2204=
NM_001457.3:c.6684C>T	NP_001448.2:p.Ile2228=
XM_005264977.1:c.6744C>T	XP_005265034.1:p.Ile2248=
XM_005264978.1:c.6705C>T	XP_005265035.1:p.Ile2235=
XM_005264978.2:c.6705C>T	XP_005265035.1:p.Ile2235=
XR_001740065.1:n.6992C>T
NM_001164317.2:c.6777C>T	NP_001157789.1:p.Ile2259=
NM_001164318.2:c.6651C>T	NP_001157790.1:p.Ile2217=
NM_001164319.2:c.6612C>T	NP_001157791.1:p.Ile2204=
NM_001457.4:c.6684C>T MANE Select	NP_001448.2:p.Ile2228=