Canonical Allele Identifier: CA15246116
Gene: FBXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33377930C>T , CM000665.2:g.33377930C>T GRCh38
NC_000003.11:g.33419422C>T , CM000665.1:g.33419422C>T GRCh37
NC_000003.10:g.33394426C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000484457.6:c.850-173C>T MANE Select ENSP00000417601.1:n.850-173C>T
ENST00000283627.10:n.862-173C>T
ENST00000421391.5:c.*479-173C>T ENSP00000408895.1:n.*479-173C>T
ENST00000422741.5:c.*628-173C>T ENSP00000406737.1:n.*628-173C>T
ENST00000432809.5:c.*530-173C>T ENSP00000411273.1:n.*530-173C>T
ENST00000435207.5:c.*889-173C>T ENSP00000411484.1:n.*889-173C>T
ENST00000451636.5:c.*674-173C>T ENSP00000416332.1:n.*674-173C>T
ENST00000463736.5:n.672-173C>T
ENST00000484457.5:c.850-173C>T ENSP00000417601.1:n.850-173C>T
ENST00000507198.5:c.646-173C>T ENSP00000426163.1:n.646-173C>T
ENST00000538892.5:c.646-173C>T ENSP00000441228.1:n.646-173C>T
NM_001171713.1:c.646-173C>T NP_001165184.1:n.646-173C>T
NM_012157.3:c.850-173C>T NP_036289.3:n.850-173C>T
XM_005265014.1:c.850-173C>T XP_005265071.1:n.850-173C>T
XM_005265015.2:c.535-173C>T XP_005265072.1:n.535-173C>T
XM_005265016.1:c.535-173C>T XP_005265073.1:n.535-173C>T
XM_005265017.2:c.535-173C>T XP_005265074.1:n.535-173C>T
XM_011533559.1:c.535-173C>T XP_011531861.1:n.535-173C>T
XR_427262.2:n.921-173C>T
NM_001349316.1:c.850-173C>T NP_001336245.1:n.850-173C>T
NM_001349319.1:c.535-173C>T NP_001336248.1:n.535-173C>T
NM_001349320.1:c.535-173C>T NP_001336249.1:n.535-173C>T
NM_001349321.1:c.535-173C>T NP_001336250.1:n.535-173C>T
NM_001349322.1:c.598-173C>T NP_001336251.1:n.598-173C>T
NM_001349323.1:c.535-173C>T NP_001336252.1:n.535-173C>T
NM_001349324.1:c.535-173C>T NP_001336253.1:n.535-173C>T
NM_001349325.1:c.535-173C>T NP_001336254.1:n.535-173C>T
NM_001349326.1:c.535-173C>T NP_001336255.1:n.535-173C>T
NM_012157.4:c.850-173C>T NP_036289.3:n.850-173C>T
NR_146121.1:n.919-173C>T
NR_146122.1:n.1013-173C>T
NR_146123.1:n.1041-173C>T
NR_146124.1:n.966-173C>T
NR_146125.1:n.1041-173C>T
NR_146126.1:n.1025-173C>T
NR_146127.1:n.947-173C>T
NR_146128.1:n.722-173C>T
NR_146129.1:n.998-173C>T
NR_146130.1:n.1112-173C>T
NR_146131.1:n.1041-173C>T
NR_146132.1:n.947-173C>T
NR_146133.1:n.997-173C>T
NR_146134.1:n.1041-173C>T
NR_146135.1:n.1034-173C>T
XM_005265015.3:c.535-173C>T XP_005265072.1:n.535-173C>T
XM_011533559.2:c.535-173C>T XP_011531861.1:n.535-173C>T
XM_017006093.1:c.535-173C>T XP_016861582.1:n.535-173C>T
XM_024453440.1:c.850-173C>T XP_024309208.1:n.850-173C>T
NM_001349316.2:c.850-173C>T NP_001336245.1:n.850-173C>T
NM_001349320.2:c.535-173C>T NP_001336249.1:n.535-173C>T
NM_001349321.2:c.535-173C>T NP_001336250.1:n.535-173C>T
NM_001349322.2:c.598-173C>T NP_001336251.1:n.598-173C>T
NM_001349324.2:c.535-173C>T NP_001336253.1:n.535-173C>T
NM_001349325.2:c.535-173C>T NP_001336254.1:n.535-173C>T
NM_001349326.2:c.535-173C>T NP_001336255.1:n.535-173C>T
NM_012157.5:c.850-173C>T MANE Select NP_036289.3:n.850-173C>T
NR_146123.2:n.1015-173C>T
NR_146126.2:n.999-173C>T
NR_146130.2:n.1086-173C>T
NR_146131.2:n.1015-173C>T
NR_146132.2:n.921-173C>T
NR_146133.2:n.971-173C>T
NR_146134.2:n.1015-173C>T
NR_146135.2:n.1008-173C>T
NM_001349319.2:c.535-173C>T NP_001336248.1:n.535-173C>T
NM_001349323.2:c.535-173C>T NP_001336252.1:n.535-173C>T
NR_146121.2:n.919-173C>T
NR_146122.2:n.1013-173C>T
NR_146124.2:n.940-173C>T
NR_146125.2:n.1015-173C>T
NR_146127.2:n.921-173C>T
NR_146128.2:n.696-173C>T
NR_146129.2:n.972-173C>T
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