Canonical Allele Identifier: CA2469456

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58154798C>T , CM000665.2:g.58154798C>T	GRCh38
NC_000003.11:g.58140525C>T , CM000665.1:g.58140525C>T	GRCh37
NC_000003.10:g.58115565C>T	NCBI36
NG_012801.1:g.151399C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.1994C>T
ENST00000682503.1:n.842C>T
ENST00000682871.1:c.6522C>T	ENSP00000507805.1:p.Phe2174=
ENST00000683114.1:n.1313C>T
ENST00000684439.1:n.2953C>T
ENST00000684506.1:c.*5195C>T	ENSP00000507728.1:n.*5195C>T
ENST00000684607.1:c.6663C>T	ENSP00000508224.1:p.Phe2221=
ENST00000295956.9:c.6642C>T MANE Select	ENSP00000295956.5:p.Phe2214=
ENST00000295956.8:c.6642C>T	ENSP00000295956.4:p.Phe2214=
ENST00000358537.7:c.6570C>T	ENSP00000351339.3:p.Phe2190=
ENST00000429972.6:c.6609C>T	ENSP00000415599.2:p.Phe2203=
ENST00000468939.1:n.189C>T
ENST00000481470.5:n.2910C>T
ENST00000490882.5:c.6735C>T	ENSP00000420213.1:p.Phe2245=
ENST00000493452.5:c.6063C>T	ENSP00000418510.1:p.Phe2021=
NM_001164317.1:c.6735C>T	NP_001157789.1:p.Phe2245=
NM_001164318.1:c.6609C>T	NP_001157790.1:p.Phe2203=
NM_001164319.1:c.6570C>T	NP_001157791.1:p.Phe2190=
NM_001457.3:c.6642C>T	NP_001448.2:p.Phe2214=
XM_005264977.1:c.6702C>T	XP_005265034.1:p.Phe2234=
XM_005264978.1:c.6663C>T	XP_005265035.1:p.Phe2221=
XM_005264978.2:c.6663C>T	XP_005265035.1:p.Phe2221=
XR_001740065.1:n.6950C>T
NM_001164317.2:c.6735C>T	NP_001157789.1:p.Phe2245=
NM_001164318.2:c.6609C>T	NP_001157790.1:p.Phe2203=
NM_001164319.2:c.6570C>T	NP_001157791.1:p.Phe2190=
NM_001457.4:c.6642C>T MANE Select	NP_001448.2:p.Phe2214=