Canonical Allele Identifier: CA108586059

Gene: FBXW7

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.152322172G>C , CM000666.2:g.152322172G>C	GRCh38
NC_000004.11:g.153243324G>C , CM000666.1:g.153243324G>C	GRCh37
NC_000004.10:g.153462774G>C	NCBI36
NG_029466.1:g.217849C>G
NG_029466.2:g.219702C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281708.10:c.*709C>G MANE Select	ENSP00000281708.3:n.*709C>G
ENST00000296555.11:c.*709C>G	ENSP00000296555.4:n.*709C>G
ENST00000393956.9:c.*709C>G	ENSP00000377528.4:n.*709C>G
ENST00000603548.6:c.*709C>G	ENSP00000474725.1:n.*709C>G
ENST00000263981.9:c.*709C>G	ENSP00000263981.4:n.*709C>G
ENST00000281708.8:c.*709C>G	ENSP00000281708.3:n.*709C>G
ENST00000296555.9:c.*709C>G	ENSP00000296555.4:n.*709C>G
NM_001013415.1:c.*709C>G	NP_001013433.1:n.*709C>G
NM_018315.4:c.*709C>G	NP_060785.2:n.*709C>G
NM_033632.3:c.*709C>G	NP_361014.1:n.*709C>G
XM_011532083.1:c.*709C>G	XP_011530385.1:n.*709C>G
XM_011532084.1:c.*709C>G	XP_011530386.1:n.*709C>G
XM_011532085.1:c.*709C>G	XP_011530387.1:n.*709C>G
XM_011532086.1:c.*709C>G	XP_011530388.1:n.*709C>G
XM_011532087.1:c.*709C>G	XP_011530389.1:n.*709C>G
XM_011532088.1:c.*709C>G	XP_011530390.1:n.*709C>G
NM_001013415.2:c.*709C>G	NP_001013433.1:n.*709C>G
NM_001349798.2:c.*709C>G MANE Select	NP_001336727.1:n.*709C>G
NM_018315.5:c.*709C>G	NP_060785.2:n.*709C>G
XM_011532084.2:c.*709C>G	XP_011530386.1:n.*709C>G
XM_011532085.2:c.*709C>G	XP_011530387.1:n.*709C>G
XM_011532086.2:c.*709C>G	XP_011530388.1:n.*709C>G
XM_011532087.2:c.*709C>G	XP_011530389.1:n.*709C>G
XM_011532088.2:c.*709C>G	XP_011530390.1:n.*709C>G
XM_024454121.1:c.*709C>G	XP_024309889.1:n.*709C>G
XM_024454122.1:c.*709C>G	XP_024309890.1:n.*709C>G
XM_024454123.1:c.*709C>G	XP_024309891.1:n.*709C>G
XM_024454124.1:c.*709C>G	XP_024309892.1:n.*709C>G
XM_024454125.1:c.*709C>G	XP_024309893.1:n.*709C>G
XM_024454126.1:c.*709C>G	XP_024309894.1:n.*709C>G