Canonical Allele Identifier: CA16618006

Gene: FLNB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58145949C>A , CM000665.2:g.58145949C>A	GRCh38
NC_000003.11:g.58131676C>A , CM000665.1:g.58131676C>A	GRCh37
NC_000003.10:g.58106716C>A	NCBI36
NG_012801.1:g.142550C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.806C>A
ENST00000682871.1:c.5334C>A	ENSP00000507805.1:p.Tyr1778Ter
ENST00000683925.1:n.1552C>A
ENST00000684439.1:n.1765C>A
ENST00000684506.1:c.*4007C>A	ENSP00000507728.1:n.*4007C>A
ENST00000684607.1:c.5475C>A	ENSP00000508224.1:p.Tyr1825Ter
ENST00000295956.9:c.5454C>A MANE Select	ENSP00000295956.5:p.Tyr1818Ter
ENST00000295956.8:c.5454C>A	ENSP00000295956.4:p.Tyr1818Ter
ENST00000358537.7:c.5382C>A	ENSP00000351339.3:p.Tyr1794Ter
ENST00000429972.6:c.5421C>A	ENSP00000415599.2:p.Tyr1807Ter
ENST00000481470.5:n.1722C>A
ENST00000490882.5:c.5547C>A	ENSP00000420213.1:p.Tyr1849Ter
ENST00000493452.5:c.4875C>A	ENSP00000418510.1:p.Tyr1625Ter
NM_001164317.1:c.5547C>A	NP_001157789.1:p.Tyr1849Ter
NM_001164318.1:c.5421C>A	NP_001157790.1:p.Tyr1807Ter
NM_001164319.1:c.5382C>A	NP_001157791.1:p.Tyr1794Ter
NM_001457.3:c.5454C>A	NP_001448.2:p.Tyr1818Ter
XM_005264977.1:c.5514C>A	XP_005265034.1:p.Tyr1838Ter
XM_005264978.1:c.5475C>A	XP_005265035.1:p.Tyr1825Ter
XM_005264981.1:c.5547C>A	XP_005265038.1:p.Tyr1849Ter
XR_940396.1:n.5692C>A
XM_005264978.2:c.5475C>A	XP_005265035.1:p.Tyr1825Ter
XR_001740065.1:n.5692C>A
XR_940396.2:n.5692C>A
NM_001164317.2:c.5547C>A	NP_001157789.1:p.Tyr1849Ter
NM_001164318.2:c.5421C>A	NP_001157790.1:p.Tyr1807Ter
NM_001164319.2:c.5382C>A	NP_001157791.1:p.Tyr1794Ter
NM_001457.4:c.5454C>A MANE Select	NP_001448.2:p.Tyr1818Ter