Canonical Allele Identifier: CA1367512583

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58136267_58136269delinsACG , CM000665.2:g.58136267_58136269delinsACG	GRCh38
NC_000003.11:g.58121994_58121996delinsACG , CM000665.1:g.58121994_58121996delinsACG	GRCh37
NC_000003.10:g.58097034_58097036delinsACG	NCBI36
NG_012801.1:g.132868_132870delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.285+99_285+101delinsACG
ENST00000682868.1:n.6903+99_6903+101delinsACG
ENST00000682871.1:c.4954+99_4954+101delinsACG	ENSP00000507805.1:n.4954+99_4954+101delinsACG
ENST00000684506.1:c.*3486+99_*3486+101delinsACG	ENSP00000507728.1:n.*3486+99_*3486+101delinsACG
ENST00000684607.1:c.4954+99_4954+101delinsACG	ENSP00000508224.1:n.4954+99_4954+101delinsACG
ENST00000295956.9:c.4861+99_4861+101delinsACG MANE Select	ENSP00000295956.5:n.4861+99_4861+101delinsACG
ENST00000295956.8:c.4861+99_4861+101delinsACG	ENSP00000295956.4:n.4861+99_4861+101delinsACG
ENST00000358537.7:c.4861+99_4861+101delinsACG	ENSP00000351339.3:n.4861+99_4861+101delinsACG
ENST00000429972.6:c.4861+99_4861+101delinsACG	ENSP00000415599.2:n.4861+99_4861+101delinsACG
ENST00000481470.5:n.1201+99_1201+101delinsACG
ENST00000490882.5:c.4954+99_4954+101delinsACG	ENSP00000420213.1:n.4954+99_4954+101delinsACG
ENST00000493452.5:c.4354+99_4354+101delinsACG	ENSP00000418510.1:n.4354+99_4354+101delinsACG
NM_001164317.1:c.4954+99_4954+101delinsACG	NP_001157789.1:n.4954+99_4954+101delinsACG
NM_001164318.1:c.4861+99_4861+101delinsACG	NP_001157790.1:n.4861+99_4861+101delinsACG
NM_001164319.1:c.4861+99_4861+101delinsACG	NP_001157791.1:n.4861+99_4861+101delinsACG
NM_001457.3:c.4861+99_4861+101delinsACG	NP_001448.2:n.4861+99_4861+101delinsACG
XM_005264977.1:c.4954+99_4954+101delinsACG	XP_005265034.1:n.4954+99_4954+101delinsACG
XM_005264978.1:c.4954+99_4954+101delinsACG	XP_005265035.1:n.4954+99_4954+101delinsACG
XM_005264981.1:c.4954+99_4954+101delinsACG	XP_005265038.1:n.4954+99_4954+101delinsACG
XR_940396.1:n.5099+99_5099+101delinsACG
XM_005264978.2:c.4954+99_4954+101delinsACG	XP_005265035.1:n.4954+99_4954+101delinsACG
XR_001740065.1:n.5099+99_5099+101delinsACG
XR_940396.2:n.5099+99_5099+101delinsACG
NM_001164317.2:c.4954+99_4954+101delinsACG	NP_001157789.1:n.4954+99_4954+101delinsACG
NM_001164318.2:c.4861+99_4861+101delinsACG	NP_001157790.1:n.4861+99_4861+101delinsACG
NM_001164319.2:c.4861+99_4861+101delinsACG	NP_001157791.1:n.4861+99_4861+101delinsACG
NM_001457.4:c.4861+99_4861+101delinsACG MANE Select	NP_001448.2:n.4861+99_4861+101delinsACG