Canonical Allele Identifier: CA16602862

Gene: FBXW7

Linked Data

• ClinVar Variation Id: 376426
• ClinVar RCV Id: RCV000419073 ; RCV000419711 ; RCV000420985 ; RCV000423791 ; RCV000429788 ; RCV000430339 ; RCV000431685 ; RCV000434480 ; RCV000440442 ; RCV000441048 ; RCV000441739 ; RCV000444420
• dbSNP Id: rs149680468
• COSMIC: COSM33763 ; COSM732380 ; COSM732381 ; COSM732382 ; COSM1149853
• MyVariant Identifiers: chr4:g.153247289G>T (hg19) ; chr4:g.152326137G>T (hg38)
• PubMed: PMID:26619011

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000703551.1:c.*206C>A	ENSP00000515367.1:n.*206C>A
ENST00000703552.1:c.1012C>A	ENSP00000515368.1:p.Arg338Ser
ENST00000703553.1:c.1513C>A	ENSP00000515369.1:p.Arg505Ser
ENST00000703554.1:c.*1160C>A	ENSP00000515370.1:n.*1160C>A
ENST00000703555.1:c.*489C>A	ENSP00000515371.1:n.*489C>A
ENST00000281708.10:c.1513C>A MANE Select	ENSP00000281708.3:p.Arg505Ser
ENST00000296555.11:c.1159C>A	ENSP00000296555.4:p.Arg387Ser
ENST00000393956.9:c.1273C>A	ENSP00000377528.4:p.Arg425Ser
ENST00000603548.6:c.1513C>A	ENSP00000474725.1:p.Arg505Ser
ENST00000647183.1:n.1062C>A
ENST00000263981.9:c.1273C>A	ENSP00000263981.4:p.Arg425Ser
ENST00000281708.8:c.1513C>A	ENSP00000281708.3:p.Arg505Ser
ENST00000296555.9:c.1159C>A	ENSP00000296555.4:p.Arg387Ser
ENST00000393956.7:c.985C>A	ENSP00000377528.3:p.Arg329Ser
ENST00000603548.5:c.1513C>A	ENSP00000474725.1:p.Arg505Ser
ENST00000603821.1:n.961C>A
ENST00000603841.1:c.1513C>A	ENSP00000474971.1:p.Arg505Ser
NM_001013415.1:c.1159C>A	NP_001013433.1:p.Arg387Ser
NM_018315.4:c.1273C>A	NP_060785.2:p.Arg425Ser
NM_033632.3:c.1513C>A	NP_361014.1:p.Arg505Ser
XM_011532083.1:c.1513C>A	XP_011530385.1:p.Arg505Ser
XM_011532084.1:c.1513C>A	XP_011530386.1:p.Arg505Ser
XM_011532085.1:c.1513C>A	XP_011530387.1:p.Arg505Ser
XM_011532086.1:c.1429C>A	XP_011530388.1:p.Arg477Ser
XM_011532087.1:c.1429C>A	XP_011530389.1:p.Arg477Ser
XM_011532088.1:c.1012C>A	XP_011530390.1:p.Arg338Ser
NM_001013415.2:c.1159C>A	NP_001013433.1:p.Arg387Ser
NM_001349798.2:c.1513C>A MANE Select	NP_001336727.1:p.Arg505Ser
NM_018315.5:c.1273C>A	NP_060785.2:p.Arg425Ser
XM_011532084.2:c.1513C>A	XP_011530386.1:p.Arg505Ser
XM_011532085.2:c.1513C>A	XP_011530387.1:p.Arg505Ser
XM_011532086.2:c.1429C>A	XP_011530388.1:p.Arg477Ser
XM_011532087.2:c.1429C>A	XP_011530389.1:p.Arg477Ser
XM_011532088.2:c.1012C>A	XP_011530390.1:p.Arg338Ser
XM_024454121.1:c.1513C>A	XP_024309889.1:p.Arg505Ser
XM_024454122.1:c.1513C>A	XP_024309890.1:p.Arg505Ser
XM_024454123.1:c.1513C>A	XP_024309891.1:p.Arg505Ser
XM_024454124.1:c.1513C>A	XP_024309892.1:p.Arg505Ser
XM_024454125.1:c.1429C>A	XP_024309893.1:p.Arg477Ser
XM_024454126.1:c.1012C>A	XP_024309894.1:p.Arg338Ser