Canonical Allele Identifier: CA16602253

Gene: FBXW7

Linked Data

• ClinVar Variation Id: 69961
• ClinVar RCV Id: RCV000422076 ; RCV000422275 ; RCV000426925 ; RCV000427176 ; RCV000428536 ; RCV000432318 ; RCV000433395 ; RCV000437170 ; RCV000438775 ; RCV000443061 ; RCV000444088 ; RCV000444218 ; RCV003335089
• dbSNP Id: rs149680468
• gnomAD v2: 4-153247289-G-A
• gnomAD v4: 4-152326137-G-A
• COSMIC: COSM22975 ; COSM74637 ; COSM108571 ; COSM108572 ; COSM1154290
• MyVariant Identifiers: chr4:g.153247289G>A (hg19) ; chr4:g.152326137G>A (hg38)
• PubMed: PMID:26619011

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000703551.1:c.*206C>T	ENSP00000515367.1:n.*206C>T
ENST00000703552.1:c.1012C>T	ENSP00000515368.1:p.Arg338Cys
ENST00000703553.1:c.1513C>T	ENSP00000515369.1:p.Arg505Cys
ENST00000703554.1:c.*1160C>T	ENSP00000515370.1:n.*1160C>T
ENST00000703555.1:c.*489C>T	ENSP00000515371.1:n.*489C>T
ENST00000281708.10:c.1513C>T MANE Select	ENSP00000281708.3:p.Arg505Cys
ENST00000296555.11:c.1159C>T	ENSP00000296555.4:p.Arg387Cys
ENST00000393956.9:c.1273C>T	ENSP00000377528.4:p.Arg425Cys
ENST00000603548.6:c.1513C>T	ENSP00000474725.1:p.Arg505Cys
ENST00000647183.1:n.1062C>T
ENST00000263981.9:c.1273C>T	ENSP00000263981.4:p.Arg425Cys
ENST00000281708.8:c.1513C>T	ENSP00000281708.3:p.Arg505Cys
ENST00000296555.9:c.1159C>T	ENSP00000296555.4:p.Arg387Cys
ENST00000393956.7:c.985C>T	ENSP00000377528.3:p.Arg329Cys
ENST00000603548.5:c.1513C>T	ENSP00000474725.1:p.Arg505Cys
ENST00000603821.1:n.961C>T
ENST00000603841.1:c.1513C>T	ENSP00000474971.1:p.Arg505Cys
NM_001013415.1:c.1159C>T	NP_001013433.1:p.Arg387Cys
NM_018315.4:c.1273C>T	NP_060785.2:p.Arg425Cys
NM_033632.3:c.1513C>T	NP_361014.1:p.Arg505Cys
XM_011532083.1:c.1513C>T	XP_011530385.1:p.Arg505Cys
XM_011532084.1:c.1513C>T	XP_011530386.1:p.Arg505Cys
XM_011532085.1:c.1513C>T	XP_011530387.1:p.Arg505Cys
XM_011532086.1:c.1429C>T	XP_011530388.1:p.Arg477Cys
XM_011532087.1:c.1429C>T	XP_011530389.1:p.Arg477Cys
XM_011532088.1:c.1012C>T	XP_011530390.1:p.Arg338Cys
NM_001013415.2:c.1159C>T	NP_001013433.1:p.Arg387Cys
NM_001349798.2:c.1513C>T MANE Select	NP_001336727.1:p.Arg505Cys
NM_018315.5:c.1273C>T	NP_060785.2:p.Arg425Cys
XM_011532084.2:c.1513C>T	XP_011530386.1:p.Arg505Cys
XM_011532085.2:c.1513C>T	XP_011530387.1:p.Arg505Cys
XM_011532086.2:c.1429C>T	XP_011530388.1:p.Arg477Cys
XM_011532087.2:c.1429C>T	XP_011530389.1:p.Arg477Cys
XM_011532088.2:c.1012C>T	XP_011530390.1:p.Arg338Cys
XM_024454121.1:c.1513C>T	XP_024309889.1:p.Arg505Cys
XM_024454122.1:c.1513C>T	XP_024309890.1:p.Arg505Cys
XM_024454123.1:c.1513C>T	XP_024309891.1:p.Arg505Cys
XM_024454124.1:c.1513C>T	XP_024309892.1:p.Arg505Cys
XM_024454125.1:c.1429C>T	XP_024309893.1:p.Arg477Cys
XM_024454126.1:c.1012C>T	XP_024309894.1:p.Arg338Cys