Canonical Allele Identifier: CA2586965842

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58077200_58077211del , CM000665.2:g.58077200_58077211del	GRCh38
NC_000003.11:g.58062927_58062938del , CM000665.1:g.58062927_58062938del	GRCh37
NC_000003.10:g.58037967_58037978del	NCBI36
NG_012801.1:g.73801_73812del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682097.1:c.447_458del	ENSP00000508183.1:p.Gln150_Ile153del
ENST00000682868.1:n.590_601del
ENST00000682871.1:c.447_458del	ENSP00000507805.1:p.Gln150_Ile153del
ENST00000682987.1:n.590_601del
ENST00000683511.1:n.606_617del
ENST00000684107.1:c.447_458del	ENSP00000507440.1:p.Gln150_Ile153del
ENST00000684506.1:c.447_458del	ENSP00000507728.1:p.Gln150_Ile153del
ENST00000684517.1:c.447_458del	ENSP00000507828.1:p.Gln150_Ile153del
ENST00000684607.1:c.447_458del	ENSP00000508224.1:p.Gln150_Ile153del
ENST00000295956.9:c.447_458del MANE Select	ENSP00000295956.5:p.Gln150_Ile153del
ENST00000295956.8:c.447_458del	ENSP00000295956.4:p.Gln150_Ile153del
ENST00000358537.7:c.447_458del	ENSP00000351339.3:p.Gln150_Ile153del
ENST00000429972.6:c.447_458del	ENSP00000415599.2:p.Gln150_Ile153del
ENST00000490882.5:c.447_458del	ENSP00000420213.1:p.Gln150_Ile153del
NM_001164317.1:c.447_458del	NP_001157789.1:p.Gln150_Ile153del
NM_001164318.1:c.447_458del	NP_001157790.1:p.Gln150_Ile153del
NM_001164319.1:c.447_458del	NP_001157791.1:p.Gln150_Ile153del
NM_001457.3:c.447_458del	NP_001448.2:p.Gln150_Ile153del
XM_005264977.1:c.447_458del	XP_005265034.1:p.Gln150_Ile153del
XM_005264978.1:c.447_458del	XP_005265035.1:p.Gln150_Ile153del
XM_005264981.1:c.447_458del	XP_005265038.1:p.Gln150_Ile153del
XR_940396.1:n.592_603del
XM_005264978.2:c.447_458del	XP_005265035.1:p.Gln150_Ile153del
XR_001740065.1:n.592_603del
XR_940396.2:n.592_603del
NM_001164317.2:c.447_458del	NP_001157789.1:p.Gln150_Ile153del
NM_001164318.2:c.447_458del	NP_001157790.1:p.Gln150_Ile153del
NM_001164319.2:c.447_458del	NP_001157791.1:p.Gln150_Ile153del
NM_001457.4:c.447_458del MANE Select	NP_001448.2:p.Gln150_Ile153del