Canonical Allele Identifier: CA16602859

Gene: FBXW7

Linked Data

• ClinVar Variation Id: 376423
• ClinVar RCV Id: RCV000419644 ; RCV000420774 ; RCV000420999 ; RCV000425337 ; RCV000426495 ; RCV000430756 ; RCV000431005 ; RCV000436496 ; RCV000437332 ; RCV000437528 ; RCV000438652 ; RCV000443509
• dbSNP Id: rs149680468
• COSMIC: COSM99603 ; COSM99604 ; COSM99605 ; COSM99606 ; COSM1133711
• MyVariant Identifiers: chr4:g.153247289G>C (hg19) ; chr4:g.152326137G>C (hg38)
• PubMed: PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.152326137G>C , CM000666.2:g.152326137G>C	GRCh38
NC_000004.11:g.153247289G>C , CM000666.1:g.153247289G>C	GRCh37
NC_000004.10:g.153466739G>C	NCBI36
NG_029466.1:g.213884C>G
NG_029466.2:g.215737C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703551.1:c.*206C>G	ENSP00000515367.1:n.*206C>G
ENST00000703552.1:c.1012C>G	ENSP00000515368.1:p.Arg338Gly
ENST00000703553.1:c.1513C>G	ENSP00000515369.1:p.Arg505Gly
ENST00000703554.1:c.*1160C>G	ENSP00000515370.1:n.*1160C>G
ENST00000703555.1:c.*489C>G	ENSP00000515371.1:n.*489C>G
ENST00000281708.10:c.1513C>G MANE Select	ENSP00000281708.3:p.Arg505Gly
ENST00000296555.11:c.1159C>G	ENSP00000296555.4:p.Arg387Gly
ENST00000393956.9:c.1273C>G	ENSP00000377528.4:p.Arg425Gly
ENST00000603548.6:c.1513C>G	ENSP00000474725.1:p.Arg505Gly
ENST00000647183.1:n.1062C>G
ENST00000263981.9:c.1273C>G	ENSP00000263981.4:p.Arg425Gly
ENST00000281708.8:c.1513C>G	ENSP00000281708.3:p.Arg505Gly
ENST00000296555.9:c.1159C>G	ENSP00000296555.4:p.Arg387Gly
ENST00000393956.7:c.985C>G	ENSP00000377528.3:p.Arg329Gly
ENST00000603548.5:c.1513C>G	ENSP00000474725.1:p.Arg505Gly
ENST00000603821.1:n.961C>G
ENST00000603841.1:c.1513C>G	ENSP00000474971.1:p.Arg505Gly
NM_001013415.1:c.1159C>G	NP_001013433.1:p.Arg387Gly
NM_018315.4:c.1273C>G	NP_060785.2:p.Arg425Gly
NM_033632.3:c.1513C>G	NP_361014.1:p.Arg505Gly
XM_011532083.1:c.1513C>G	XP_011530385.1:p.Arg505Gly
XM_011532084.1:c.1513C>G	XP_011530386.1:p.Arg505Gly
XM_011532085.1:c.1513C>G	XP_011530387.1:p.Arg505Gly
XM_011532086.1:c.1429C>G	XP_011530388.1:p.Arg477Gly
XM_011532087.1:c.1429C>G	XP_011530389.1:p.Arg477Gly
XM_011532088.1:c.1012C>G	XP_011530390.1:p.Arg338Gly
NM_001013415.2:c.1159C>G	NP_001013433.1:p.Arg387Gly
NM_001349798.2:c.1513C>G MANE Select	NP_001336727.1:p.Arg505Gly
NM_018315.5:c.1273C>G	NP_060785.2:p.Arg425Gly
XM_011532084.2:c.1513C>G	XP_011530386.1:p.Arg505Gly
XM_011532085.2:c.1513C>G	XP_011530387.1:p.Arg505Gly
XM_011532086.2:c.1429C>G	XP_011530388.1:p.Arg477Gly
XM_011532087.2:c.1429C>G	XP_011530389.1:p.Arg477Gly
XM_011532088.2:c.1012C>G	XP_011530390.1:p.Arg338Gly
XM_024454121.1:c.1513C>G	XP_024309889.1:p.Arg505Gly
XM_024454122.1:c.1513C>G	XP_024309890.1:p.Arg505Gly
XM_024454123.1:c.1513C>G	XP_024309891.1:p.Arg505Gly
XM_024454124.1:c.1513C>G	XP_024309892.1:p.Arg505Gly
XM_024454125.1:c.1429C>G	XP_024309893.1:p.Arg477Gly
XM_024454126.1:c.1012C>G	XP_024309894.1:p.Arg338Gly