Canonical Allele Identifier: CA353359787

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58153623G>C , CM000665.2:g.58153623G>C	GRCh38
NC_000003.11:g.58139350G>C , CM000665.1:g.58139350G>C	GRCh37
NC_000003.10:g.58114390G>C	NCBI36
NG_012801.1:g.150224G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.1968G>C
ENST00000682503.1:n.816G>C
ENST00000682871.1:c.6496G>C	ENSP00000507805.1:p.Gly2166Arg
ENST00000683114.1:n.1287G>C
ENST00000684439.1:n.2927G>C
ENST00000684506.1:c.*5169G>C	ENSP00000507728.1:n.*5169G>C
ENST00000684607.1:c.6637G>C	ENSP00000508224.1:p.Gly2213Arg
ENST00000295956.9:c.6616G>C MANE Select	ENSP00000295956.5:p.Gly2206Arg
ENST00000295956.8:c.6616G>C	ENSP00000295956.4:p.Gly2206Arg
ENST00000358537.7:c.6544G>C	ENSP00000351339.3:p.Gly2182Arg
ENST00000429972.6:c.6583G>C	ENSP00000415599.2:p.Gly2195Arg
ENST00000466455.1:c.386G>C
ENST00000481470.5:n.2884G>C
ENST00000490882.5:c.6709G>C	ENSP00000420213.1:p.Gly2237Arg
ENST00000493452.5:c.6037G>C	ENSP00000418510.1:p.Gly2013Arg
NM_001164317.1:c.6709G>C	NP_001157789.1:p.Gly2237Arg
NM_001164318.1:c.6583G>C	NP_001157790.1:p.Gly2195Arg
NM_001164319.1:c.6544G>C	NP_001157791.1:p.Gly2182Arg
NM_001457.3:c.6616G>C	NP_001448.2:p.Gly2206Arg
XM_005264977.1:c.6676G>C	XP_005265034.1:p.Gly2226Arg
XM_005264978.1:c.6637G>C	XP_005265035.1:p.Gly2213Arg
XM_005264978.2:c.6637G>C	XP_005265035.1:p.Gly2213Arg
XR_001740065.1:n.6924G>C
NM_001164317.2:c.6709G>C	NP_001157789.1:p.Gly2237Arg
NM_001164318.2:c.6583G>C	NP_001157790.1:p.Gly2195Arg
NM_001164319.2:c.6544G>C	NP_001157791.1:p.Gly2182Arg
NM_001457.4:c.6616G>C MANE Select	NP_001448.2:p.Gly2206Arg