Canonical Allele Identifier: CA1367512464

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58136052_58136055delinsCCGA , CM000665.2:g.58136052_58136055delinsCCGA	GRCh38
NC_000003.11:g.58121779_58121782delinsCCGA , CM000665.1:g.58121779_58121782delinsCCGA	GRCh37
NC_000003.10:g.58096819_58096822delinsCCGA	NCBI36
NG_012801.1:g.132653_132656delinsCCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.169_172delinsCCGA
ENST00000682868.1:n.6787_6790delinsCCGA
ENST00000682871.1:c.4838_4841delinsCCGA	ENSP00000507805.1:p.Pro1613=
ENST00000684506.1:c.*3370_*3373delinsCCGA	ENSP00000507728.1:n.*3370_*3373delinsCCGA
ENST00000684607.1:c.4838_4841delinsCCGA	ENSP00000508224.1:p.Pro1613=
ENST00000295956.9:c.4745_4748delinsCCGA MANE Select	ENSP00000295956.5:p.Pro1582=
ENST00000295956.8:c.4745_4748delinsCCGA	ENSP00000295956.4:p.Pro1582=
ENST00000358537.7:c.4745_4748delinsCCGA	ENSP00000351339.3:p.Pro1582=
ENST00000429972.6:c.4745_4748delinsCCGA	ENSP00000415599.2:p.Pro1582=
ENST00000481470.5:n.1085_1088delinsCCGA
ENST00000490882.5:c.4838_4841delinsCCGA	ENSP00000420213.1:p.Pro1613=
ENST00000493452.5:c.4238_4241delinsCCGA	ENSP00000418510.1:p.Pro1413=
NM_001164317.1:c.4838_4841delinsCCGA	NP_001157789.1:p.Pro1613=
NM_001164318.1:c.4745_4748delinsCCGA	NP_001157790.1:p.Pro1582=
NM_001164319.1:c.4745_4748delinsCCGA	NP_001157791.1:p.Pro1582=
NM_001457.3:c.4745_4748delinsCCGA	NP_001448.2:p.Pro1582=
XM_005264977.1:c.4838_4841delinsCCGA	XP_005265034.1:p.Pro1613=
XM_005264978.1:c.4838_4841delinsCCGA	XP_005265035.1:p.Pro1613=
XM_005264981.1:c.4838_4841delinsCCGA	XP_005265038.1:p.Pro1613=
XR_940396.1:n.4983_4986delinsCCGA
XM_005264978.2:c.4838_4841delinsCCGA	XP_005265035.1:p.Pro1613=
XR_001740065.1:n.4983_4986delinsCCGA
XR_940396.2:n.4983_4986delinsCCGA
NM_001164317.2:c.4838_4841delinsCCGA	NP_001157789.1:p.Pro1613=
NM_001164318.2:c.4745_4748delinsCCGA	NP_001157790.1:p.Pro1582=
NM_001164319.2:c.4745_4748delinsCCGA	NP_001157791.1:p.Pro1582=
NM_001457.4:c.4745_4748delinsCCGA MANE Select	NP_001448.2:p.Pro1582=