Canonical Allele Identifier: CA353354716

Gene: FLNB

Linked Data

• MyVariant Identifiers: chr3:g.58131725G>A (hg19) ; chr3:g.58145998G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58145998G>A , CM000665.2:g.58145998G>A	GRCh38
NC_000003.11:g.58131725G>A , CM000665.1:g.58131725G>A	GRCh37
NC_000003.10:g.58106765G>A	NCBI36
NG_012801.1:g.142599G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682297.1:n.855G>A
ENST00000682871.1:c.5383G>A	ENSP00000507805.1:p.Val1795Met
ENST00000683925.1:n.1601G>A
ENST00000684439.1:n.1814G>A
ENST00000684506.1:c.*4056G>A	ENSP00000507728.1:n.*4056G>A
ENST00000684607.1:c.5524G>A	ENSP00000508224.1:p.Val1842Met
ENST00000295956.9:c.5503G>A MANE Select	ENSP00000295956.5:p.Val1835Met
ENST00000295956.8:c.5503G>A	ENSP00000295956.4:p.Val1835Met
ENST00000358537.7:c.5431G>A	ENSP00000351339.3:p.Val1811Met
ENST00000429972.6:c.5470G>A	ENSP00000415599.2:p.Val1824Met
ENST00000481470.5:n.1771G>A
ENST00000490882.5:c.5596G>A	ENSP00000420213.1:p.Val1866Met
ENST00000493452.5:c.4924G>A	ENSP00000418510.1:p.Val1642Met
NM_001164317.1:c.5596G>A	NP_001157789.1:p.Val1866Met
NM_001164318.1:c.5470G>A	NP_001157790.1:p.Val1824Met
NM_001164319.1:c.5431G>A	NP_001157791.1:p.Val1811Met
NM_001457.3:c.5503G>A	NP_001448.2:p.Val1835Met
XM_005264977.1:c.5563G>A	XP_005265034.1:p.Val1855Met
XM_005264978.1:c.5524G>A	XP_005265035.1:p.Val1842Met
XM_005264981.1:c.5596G>A	XP_005265038.1:p.Val1866Met
XR_940396.1:n.5741G>A
XM_005264978.2:c.5524G>A	XP_005265035.1:p.Val1842Met
XR_001740065.1:n.5741G>A
XR_940396.2:n.5741G>A
NM_001164317.2:c.5596G>A	NP_001157789.1:p.Val1866Met
NM_001164318.2:c.5470G>A	NP_001157790.1:p.Val1824Met
NM_001164319.2:c.5431G>A	NP_001157791.1:p.Val1811Met
NM_001457.4:c.5503G>A MANE Select	NP_001448.2:p.Val1835Met