Canonical Allele Identifier: CA353354556

Gene: FLNB

Linked Data

• MyVariant Identifiers: chr3:g.58131651G>C (hg19) ; chr3:g.58145924G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58145924G>C , CM000665.2:g.58145924G>C	GRCh38
NC_000003.11:g.58131651G>C , CM000665.1:g.58131651G>C	GRCh37
NC_000003.10:g.58106691G>C	NCBI36
NG_012801.1:g.142525G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682297.1:n.781G>C
ENST00000682871.1:c.5309G>C	ENSP00000507805.1:p.Ser1770Thr
ENST00000683925.1:n.1527G>C
ENST00000684439.1:n.1740G>C
ENST00000684506.1:c.*3982G>C	ENSP00000507728.1:n.*3982G>C
ENST00000684607.1:c.5450G>C	ENSP00000508224.1:p.Ser1817Thr
ENST00000295956.9:c.5429G>C MANE Select	ENSP00000295956.5:p.Ser1810Thr
ENST00000295956.8:c.5429G>C	ENSP00000295956.4:p.Ser1810Thr
ENST00000358537.7:c.5357G>C	ENSP00000351339.3:p.Ser1786Thr
ENST00000429972.6:c.5396G>C	ENSP00000415599.2:p.Ser1799Thr
ENST00000481470.5:n.1697G>C
ENST00000490882.5:c.5522G>C	ENSP00000420213.1:p.Ser1841Thr
ENST00000493452.5:c.4850G>C	ENSP00000418510.1:p.Ser1617Thr
NM_001164317.1:c.5522G>C	NP_001157789.1:p.Ser1841Thr
NM_001164318.1:c.5396G>C	NP_001157790.1:p.Ser1799Thr
NM_001164319.1:c.5357G>C	NP_001157791.1:p.Ser1786Thr
NM_001457.3:c.5429G>C	NP_001448.2:p.Ser1810Thr
XM_005264977.1:c.5489G>C	XP_005265034.1:p.Ser1830Thr
XM_005264978.1:c.5450G>C	XP_005265035.1:p.Ser1817Thr
XM_005264981.1:c.5522G>C	XP_005265038.1:p.Ser1841Thr
XR_940396.1:n.5667G>C
XM_005264978.2:c.5450G>C	XP_005265035.1:p.Ser1817Thr
XR_001740065.1:n.5667G>C
XR_940396.2:n.5667G>C
NM_001164317.2:c.5522G>C	NP_001157789.1:p.Ser1841Thr
NM_001164318.2:c.5396G>C	NP_001157790.1:p.Ser1799Thr
NM_001164319.2:c.5357G>C	NP_001157791.1:p.Ser1786Thr
NM_001457.4:c.5429G>C MANE Select	NP_001448.2:p.Ser1810Thr