Canonical Allele Identifier: CA2837997375

Gene: FBXW7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.152328233G= , CM000666.2:g.152328233G=	GRCh38
NC_000004.11:g.153249385G= , CM000666.1:g.153249385G=	GRCh37
NC_000004.10:g.153468835G=	NCBI36
NG_029466.1:g.211788C=
NG_029466.2:g.213641C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001349798.2:c.1393C= MANE Select	NP_001336727.1:p.Arg465=
ENST00000281708.10:c.1393C= MANE Select	ENSP00000281708.3:p.Arg465=
NM_001013415.1:c.1039C=	NP_001013433.1:p.Arg347=
NM_001013415.2:c.1039C=	NP_001013433.1:p.Arg347=
NM_018315.4:c.1153C=	NP_060785.2:p.Arg385=
NM_018315.5:c.1153C=	NP_060785.2:p.Arg385=
NM_033632.3:c.1393C=	NP_361014.1:p.Arg465=
ENST00000263981.9:c.1153C=	ENSP00000263981.4:p.Arg385=
ENST00000281708.8:c.1393C=	ENSP00000281708.3:p.Arg465=
ENST00000296555.11:c.1039C=	ENSP00000296555.4:p.Arg347=
ENST00000296555.9:c.1039C=	ENSP00000296555.4:p.Arg347=
ENST00000393956.7:c.865C=	ENSP00000377528.3:p.Arg289=
ENST00000393956.9:c.1153C=	ENSP00000377528.4:p.Arg385=
ENST00000603548.5:c.1393C=	ENSP00000474725.1:p.Arg465=
ENST00000603548.6:c.1393C=	ENSP00000474725.1:p.Arg465=
ENST00000603821.1:n.841C=
ENST00000603841.1:c.1393C=	ENSP00000474971.1:p.Arg465=
ENST00000604069.1:n.580C=
ENST00000647183.1:n.942C=
ENST00000703551.1:c.*86C=	ENSP00000515367.1:n.*86C=
ENST00000703552.1:c.892C=	ENSP00000515368.1:p.Arg298=
ENST00000703553.1:c.1393C=	ENSP00000515369.1:p.Arg465=
ENST00000703554.1:c.*1040C=	ENSP00000515370.1:n.*1040C=
ENST00000703555.1:c.*369C=	ENSP00000515371.1:n.*369C=
XM_011532083.1:c.1393C=	XP_011530385.1:p.Arg465=
XM_011532084.1:c.1393C=	XP_011530386.1:p.Arg465=
XM_011532084.2:c.1393C=	XP_011530386.1:p.Arg465=
XM_011532085.1:c.1393C=	XP_011530387.1:p.Arg465=
XM_011532085.2:c.1393C=	XP_011530387.1:p.Arg465=
XM_011532086.1:c.1309C=	XP_011530388.1:p.Arg437=
XM_011532086.2:c.1309C=	XP_011530388.1:p.Arg437=
XM_011532087.1:c.1309C=	XP_011530389.1:p.Arg437=
XM_011532087.2:c.1309C=	XP_011530389.1:p.Arg437=
XM_011532088.1:c.892C=	XP_011530390.1:p.Arg298=
XM_011532088.2:c.892C=	XP_011530390.1:p.Arg298=
XM_024454121.1:c.1393C=	XP_024309889.1:p.Arg465=
XM_024454122.1:c.1393C=	XP_024309890.1:p.Arg465=
XM_024454123.1:c.1393C=	XP_024309891.1:p.Arg465=
XM_024454124.1:c.1393C=	XP_024309892.1:p.Arg465=
XM_024454125.1:c.1309C=	XP_024309893.1:p.Arg437=
XM_024454126.1:c.892C=	XP_024309894.1:p.Arg298=