Canonical Allele Identifier: CA2401985342

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475246C= , CM000684.2:g.32475246C=	GRCh38
NC_000022.10:g.32871233C= , CM000684.1:g.32871233C=	GRCh37
NC_000022.9:g.31201233C=	NCBI36
NG_016001.1:g.5527C=
NG_016001.2:g.5527C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.122+122C= MANE Select	ENSP00000266087.7:n.122+122C=
ENST00000266087.11:c.122+122C=	ENSP00000266087.7:n.122+122C=
ENST00000420700.5:c.122+122C=	ENSP00000406155.1:n.122+122C=
ENST00000425028.5:c.122+122C=	ENSP00000395823.1:n.122+122C=
ENST00000452138.3:c.-116C=	ENSP00000388547.2:n.-116C=
ENST00000492535.1:n.110+122C=
NM_001033024.1:c.-116C=	NP_001028196.1:n.-116C=
NM_001257990.1:c.-373C=	NP_001244919.1:n.-373C=
NM_012179.3:c.122+122C=	NP_036311.3:n.122+122C=
XM_011530106.1:c.-52+122C=	XP_011528408.1:n.-52+122C=
XM_024452207.1:c.-69+122C=	XP_024307975.1:n.-69+122C=
NM_012179.4:c.122+122C= MANE Select	NP_036311.3:n.122+122C=