Canonical Allele Identifier: CA2401989546

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484543T= , CM000684.2:g.32484543T=	GRCh38
NC_000022.10:g.32880530T= , CM000684.1:g.32880530T=	GRCh37
NC_000022.9:g.31210530T=	NCBI36
NG_016001.1:g.14824T=
NG_016001.2:g.14824T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+419T= MANE Select	ENSP00000266087.7:n.645+419T=
ENST00000266087.11:c.645+419T=	ENSP00000266087.7:n.645+419T=
ENST00000397426.5:c.303+419T=	ENSP00000380571.1:n.303+419T=
ENST00000420700.5:c.*224+419T=	ENSP00000406155.1:n.*224+419T=
ENST00000425028.5:c.*343+419T=	ENSP00000395823.1:n.*343+419T=
ENST00000452138.3:c.408+419T=	ENSP00000388547.2:n.408+419T=
ENST00000492535.1:n.481+419T=
NM_001033024.1:c.408+419T=	NP_001028196.1:n.408+419T=
NM_001257990.1:c.303+419T=	NP_001244919.1:n.303+419T=
NM_012179.3:c.645+419T=	NP_036311.3:n.645+419T=
XM_011530106.1:c.177+419T=	XP_011528408.1:n.177+419T=
XM_024452207.1:c.303+419T=	XP_024307975.1:n.303+419T=
NM_012179.4:c.645+419T= MANE Select	NP_036311.3:n.645+419T=
NM_001033024.2:c.408+419T=	NP_001028196.1:n.408+419T=
NM_001257990.2:c.303+419T=	NP_001244919.1:n.303+419T=