Canonical Allele Identifier: CA2401989558

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484576G= , CM000684.2:g.32484576G=	GRCh38
NC_000022.10:g.32880563G= , CM000684.1:g.32880563G=	GRCh37
NC_000022.9:g.31210563G=	NCBI36
NG_016001.1:g.14857G=
NG_016001.2:g.14857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+452G= MANE Select	ENSP00000266087.7:n.645+452G=
ENST00000266087.11:c.645+452G=	ENSP00000266087.7:n.645+452G=
ENST00000397426.5:c.303+452G=	ENSP00000380571.1:n.303+452G=
ENST00000420700.5:c.*224+452G=	ENSP00000406155.1:n.*224+452G=
ENST00000425028.5:c.*343+452G=	ENSP00000395823.1:n.*343+452G=
ENST00000452138.3:c.408+452G=	ENSP00000388547.2:n.408+452G=
ENST00000492535.1:n.481+452G=
NM_001033024.1:c.408+452G=	NP_001028196.1:n.408+452G=
NM_001257990.1:c.303+452G=	NP_001244919.1:n.303+452G=
NM_012179.3:c.645+452G=	NP_036311.3:n.645+452G=
XM_011530106.1:c.177+452G=	XP_011528408.1:n.177+452G=
XM_024452207.1:c.303+452G=	XP_024307975.1:n.303+452G=
NM_012179.4:c.645+452G= MANE Select	NP_036311.3:n.645+452G=
NM_001033024.2:c.408+452G=	NP_001028196.1:n.408+452G=
NM_001257990.2:c.303+452G=	NP_001244919.1:n.303+452G=