Canonical Allele Identifier: CA358618165

Gene: FBXW7

Linked Data

• dbSNP Id: rs1057519896
• COSMIC: COSM22976 ; COSM5686715 ; COSM5686716 ; COSM5686717 ; COSM5686718
• MyVariant Identifiers: chr4:g.153247288C>G (hg19) ; chr4:g.152326136C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.152326136C>G , CM000666.2:g.152326136C>G	GRCh38
NC_000004.11:g.153247288C>G , CM000666.1:g.153247288C>G	GRCh37
NC_000004.10:g.153466738C>G	NCBI36
NG_029466.1:g.213885G>C
NG_029466.2:g.215738G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703551.1:c.*207G>C	ENSP00000515367.1:n.*207G>C
ENST00000703552.1:c.1013G>C	ENSP00000515368.1:p.Arg338Pro
ENST00000703553.1:c.1514G>C	ENSP00000515369.1:p.Arg505Pro
ENST00000703554.1:c.*1161G>C	ENSP00000515370.1:n.*1161G>C
ENST00000703555.1:c.*490G>C	ENSP00000515371.1:n.*490G>C
ENST00000281708.10:c.1514G>C MANE Select	ENSP00000281708.3:p.Arg505Pro
ENST00000296555.11:c.1160G>C	ENSP00000296555.4:p.Arg387Pro
ENST00000393956.9:c.1274G>C	ENSP00000377528.4:p.Arg425Pro
ENST00000603548.6:c.1514G>C	ENSP00000474725.1:p.Arg505Pro
ENST00000647183.1:n.1063G>C
ENST00000263981.9:c.1274G>C	ENSP00000263981.4:p.Arg425Pro
ENST00000281708.8:c.1514G>C	ENSP00000281708.3:p.Arg505Pro
ENST00000296555.9:c.1160G>C	ENSP00000296555.4:p.Arg387Pro
ENST00000393956.7:c.986G>C	ENSP00000377528.3:p.Arg329Pro
ENST00000603548.5:c.1514G>C	ENSP00000474725.1:p.Arg505Pro
ENST00000603821.1:n.962G>C
ENST00000603841.1:c.1514G>C	ENSP00000474971.1:p.Arg505Pro
NM_001013415.1:c.1160G>C	NP_001013433.1:p.Arg387Pro
NM_018315.4:c.1274G>C	NP_060785.2:p.Arg425Pro
NM_033632.3:c.1514G>C	NP_361014.1:p.Arg505Pro
XM_011532083.1:c.1514G>C	XP_011530385.1:p.Arg505Pro
XM_011532084.1:c.1514G>C	XP_011530386.1:p.Arg505Pro
XM_011532085.1:c.1514G>C	XP_011530387.1:p.Arg505Pro
XM_011532086.1:c.1430G>C	XP_011530388.1:p.Arg477Pro
XM_011532087.1:c.1430G>C	XP_011530389.1:p.Arg477Pro
XM_011532088.1:c.1013G>C	XP_011530390.1:p.Arg338Pro
NM_001013415.2:c.1160G>C	NP_001013433.1:p.Arg387Pro
NM_001349798.2:c.1514G>C MANE Select	NP_001336727.1:p.Arg505Pro
NM_018315.5:c.1274G>C	NP_060785.2:p.Arg425Pro
XM_011532084.2:c.1514G>C	XP_011530386.1:p.Arg505Pro
XM_011532085.2:c.1514G>C	XP_011530387.1:p.Arg505Pro
XM_011532086.2:c.1430G>C	XP_011530388.1:p.Arg477Pro
XM_011532087.2:c.1430G>C	XP_011530389.1:p.Arg477Pro
XM_011532088.2:c.1013G>C	XP_011530390.1:p.Arg338Pro
XM_024454121.1:c.1514G>C	XP_024309889.1:p.Arg505Pro
XM_024454122.1:c.1514G>C	XP_024309890.1:p.Arg505Pro
XM_024454123.1:c.1514G>C	XP_024309891.1:p.Arg505Pro
XM_024454124.1:c.1514G>C	XP_024309892.1:p.Arg505Pro
XM_024454125.1:c.1430G>C	XP_024309893.1:p.Arg477Pro
XM_024454126.1:c.1013G>C	XP_024309894.1:p.Arg338Pro