Canonical Allele Identifier: CA353354712

Gene: FLNB

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58145995G>C , CM000665.2:g.58145995G>C	GRCh38
NC_000003.11:g.58131722G>C , CM000665.1:g.58131722G>C	GRCh37
NC_000003.10:g.58106762G>C	NCBI36
NG_012801.1:g.142596G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.852G>C
ENST00000682871.1:c.5380G>C	ENSP00000507805.1:p.Gly1794Arg
ENST00000683925.1:n.1598G>C
ENST00000684439.1:n.1811G>C
ENST00000684506.1:c.*4053G>C	ENSP00000507728.1:n.*4053G>C
ENST00000684607.1:c.5521G>C	ENSP00000508224.1:p.Gly1841Arg
ENST00000295956.9:c.5500G>C MANE Select	ENSP00000295956.5:p.Gly1834Arg
ENST00000295956.8:c.5500G>C	ENSP00000295956.4:p.Gly1834Arg
ENST00000358537.7:c.5428G>C	ENSP00000351339.3:p.Gly1810Arg
ENST00000429972.6:c.5467G>C	ENSP00000415599.2:p.Gly1823Arg
ENST00000481470.5:n.1768G>C
ENST00000490882.5:c.5593G>C	ENSP00000420213.1:p.Gly1865Arg
ENST00000493452.5:c.4921G>C	ENSP00000418510.1:p.Gly1641Arg
NM_001164317.1:c.5593G>C	NP_001157789.1:p.Gly1865Arg
NM_001164318.1:c.5467G>C	NP_001157790.1:p.Gly1823Arg
NM_001164319.1:c.5428G>C	NP_001157791.1:p.Gly1810Arg
NM_001457.3:c.5500G>C	NP_001448.2:p.Gly1834Arg
XM_005264977.1:c.5560G>C	XP_005265034.1:p.Gly1854Arg
XM_005264978.1:c.5521G>C	XP_005265035.1:p.Gly1841Arg
XM_005264981.1:c.5593G>C	XP_005265038.1:p.Gly1865Arg
XR_940396.1:n.5738G>C
XM_005264978.2:c.5521G>C	XP_005265035.1:p.Gly1841Arg
XR_001740065.1:n.5738G>C
XR_940396.2:n.5738G>C
NM_001164317.2:c.5593G>C	NP_001157789.1:p.Gly1865Arg
NM_001164318.2:c.5467G>C	NP_001157790.1:p.Gly1823Arg
NM_001164319.2:c.5428G>C	NP_001157791.1:p.Gly1810Arg
NM_001457.4:c.5500G>C MANE Select	NP_001448.2:p.Gly1834Arg