Canonical Allele Identifier: CA2401989435

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484272A= , CM000684.2:g.32484272A=	GRCh38
NC_000022.10:g.32880259A= , CM000684.1:g.32880259A=	GRCh37
NC_000022.9:g.31210259A=	NCBI36
NG_016001.1:g.14553A=
NG_016001.2:g.14553A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+148A= MANE Select	ENSP00000266087.7:n.645+148A=
ENST00000266087.11:c.645+148A=	ENSP00000266087.7:n.645+148A=
ENST00000397426.5:c.303+148A=	ENSP00000380571.1:n.303+148A=
ENST00000420700.5:c.*224+148A=	ENSP00000406155.1:n.*224+148A=
ENST00000425028.5:c.*343+148A=	ENSP00000395823.1:n.*343+148A=
ENST00000452138.3:c.408+148A=	ENSP00000388547.2:n.408+148A=
ENST00000492535.1:n.481+148A=
NM_001033024.1:c.408+148A=	NP_001028196.1:n.408+148A=
NM_001257990.1:c.303+148A=	NP_001244919.1:n.303+148A=
NM_012179.3:c.645+148A=	NP_036311.3:n.645+148A=
XM_011530106.1:c.177+148A=	XP_011528408.1:n.177+148A=
XM_024452207.1:c.303+148A=	XP_024307975.1:n.303+148A=
NM_012179.4:c.645+148A= MANE Select	NP_036311.3:n.645+148A=
NM_001033024.2:c.408+148A=	NP_001028196.1:n.408+148A=
NM_001257990.2:c.303+148A=	NP_001244919.1:n.303+148A=