Canonical Allele Identifier: CA353354726

Gene: FLNB

Linked Data

• gnomAD v4: 3-58146004-A-G
• MyVariant Identifiers: chr3:g.58131731A>G (hg19) ; chr3:g.58146004A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58146004A>G , CM000665.2:g.58146004A>G	GRCh38
NC_000003.11:g.58131731A>G , CM000665.1:g.58131731A>G	GRCh37
NC_000003.10:g.58106771A>G	NCBI36
NG_012801.1:g.142605A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682297.1:n.861A>G
ENST00000682871.1:c.5389A>G	ENSP00000507805.1:p.Asn1797Asp
ENST00000683925.1:n.1607A>G
ENST00000684439.1:n.1820A>G
ENST00000684506.1:c.*4062A>G	ENSP00000507728.1:n.*4062A>G
ENST00000684607.1:c.5530A>G	ENSP00000508224.1:p.Asn1844Asp
ENST00000295956.9:c.5509A>G MANE Select	ENSP00000295956.5:p.Asn1837Asp
ENST00000295956.8:c.5509A>G	ENSP00000295956.4:p.Asn1837Asp
ENST00000358537.7:c.5437A>G	ENSP00000351339.3:p.Asn1813Asp
ENST00000429972.6:c.5476A>G	ENSP00000415599.2:p.Asn1826Asp
ENST00000481470.5:n.1777A>G
ENST00000490882.5:c.5602A>G	ENSP00000420213.1:p.Asn1868Asp
ENST00000493452.5:c.4930A>G	ENSP00000418510.1:p.Asn1644Asp
NM_001164317.1:c.5602A>G	NP_001157789.1:p.Asn1868Asp
NM_001164318.1:c.5476A>G	NP_001157790.1:p.Asn1826Asp
NM_001164319.1:c.5437A>G	NP_001157791.1:p.Asn1813Asp
NM_001457.3:c.5509A>G	NP_001448.2:p.Asn1837Asp
XM_005264977.1:c.5569A>G	XP_005265034.1:p.Asn1857Asp
XM_005264978.1:c.5530A>G	XP_005265035.1:p.Asn1844Asp
XM_005264981.1:c.5602A>G	XP_005265038.1:p.Asn1868Asp
XR_940396.1:n.5747A>G
XM_005264978.2:c.5530A>G	XP_005265035.1:p.Asn1844Asp
XR_001740065.1:n.5747A>G
XR_940396.2:n.5747A>G
NM_001164317.2:c.5602A>G	NP_001157789.1:p.Asn1868Asp
NM_001164318.2:c.5476A>G	NP_001157790.1:p.Asn1826Asp
NM_001164319.2:c.5437A>G	NP_001157791.1:p.Asn1813Asp
NM_001457.4:c.5509A>G MANE Select	NP_001448.2:p.Asn1837Asp