Canonical Allele Identifier: CA16602854
Gene: FBXW7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.152328232C>A , CM000666.2:g.152328232C>A GRCh38
NC_000004.11:g.153249384C>A , CM000666.1:g.153249384C>A GRCh37
NC_000004.10:g.153468834C>A NCBI36
NG_029466.1:g.211789G>T
NG_029466.2:g.213642G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703551.1:c.*87G>T ENSP00000515367.1:n.*87G>T
ENST00000703552.1:c.893G>T ENSP00000515368.1:p.Arg298Leu
ENST00000703553.1:c.1394G>T ENSP00000515369.1:p.Arg465Leu
ENST00000703554.1:c.*1041G>T ENSP00000515370.1:n.*1041G>T
ENST00000703555.1:c.*370G>T ENSP00000515371.1:n.*370G>T
ENST00000281708.10:c.1394G>T MANE Select ENSP00000281708.3:p.Arg465Leu
ENST00000296555.11:c.1040G>T ENSP00000296555.4:p.Arg347Leu
ENST00000393956.9:c.1154G>T ENSP00000377528.4:p.Arg385Leu
ENST00000603548.6:c.1394G>T ENSP00000474725.1:p.Arg465Leu
ENST00000647183.1:n.943G>T
ENST00000263981.9:c.1154G>T ENSP00000263981.4:p.Arg385Leu
ENST00000281708.8:c.1394G>T ENSP00000281708.3:p.Arg465Leu
ENST00000296555.9:c.1040G>T ENSP00000296555.4:p.Arg347Leu
ENST00000393956.7:c.866G>T ENSP00000377528.3:p.Arg289Leu
ENST00000603548.5:c.1394G>T ENSP00000474725.1:p.Arg465Leu
ENST00000603821.1:n.842G>T
ENST00000603841.1:c.1394G>T ENSP00000474971.1:p.Arg465Leu
ENST00000604069.1:n.581G>T
NM_001013415.1:c.1040G>T NP_001013433.1:p.Arg347Leu
NM_018315.4:c.1154G>T NP_060785.2:p.Arg385Leu
NM_033632.3:c.1394G>T NP_361014.1:p.Arg465Leu
XM_011532083.1:c.1394G>T XP_011530385.1:p.Arg465Leu
XM_011532084.1:c.1394G>T XP_011530386.1:p.Arg465Leu
XM_011532085.1:c.1394G>T XP_011530387.1:p.Arg465Leu
XM_011532086.1:c.1310G>T XP_011530388.1:p.Arg437Leu
XM_011532087.1:c.1310G>T XP_011530389.1:p.Arg437Leu
XM_011532088.1:c.893G>T XP_011530390.1:p.Arg298Leu
NM_001013415.2:c.1040G>T NP_001013433.1:p.Arg347Leu
NM_001349798.2:c.1394G>T MANE Select NP_001336727.1:p.Arg465Leu
NM_018315.5:c.1154G>T NP_060785.2:p.Arg385Leu
XM_011532084.2:c.1394G>T XP_011530386.1:p.Arg465Leu
XM_011532085.2:c.1394G>T XP_011530387.1:p.Arg465Leu
XM_011532086.2:c.1310G>T XP_011530388.1:p.Arg437Leu
XM_011532087.2:c.1310G>T XP_011530389.1:p.Arg437Leu
XM_011532088.2:c.893G>T XP_011530390.1:p.Arg298Leu
XM_024454121.1:c.1394G>T XP_024309889.1:p.Arg465Leu
XM_024454122.1:c.1394G>T XP_024309890.1:p.Arg465Leu
XM_024454123.1:c.1394G>T XP_024309891.1:p.Arg465Leu
XM_024454124.1:c.1394G>T XP_024309892.1:p.Arg465Leu
XM_024454125.1:c.1310G>T XP_024309893.1:p.Arg437Leu
XM_024454126.1:c.893G>T XP_024309894.1:p.Arg298Leu