Canonical Allele Identifier: CA2580095011
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713937
ClinVar RCV Id: RCV002296920

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7675202_7675203delinsTC , CM000679.2:g.7675202_7675203delinsTC GRCh38
NC_000017.10:g.7578520_7578521delinsTC , CM000679.1:g.7578520_7578521delinsTC GRCh37
NC_000017.9:g.7519245_7519246delinsTC NCBI36
NG_017013.2:g.17348_17349delinsGA , LRG_321:g.17348_17349delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.409_410delinsGA ENSP00000426252.2:p.Leu137Glu
ENST00000508793.6:c.409_410delinsGA ENSP00000424104.2:p.Leu137Glu
ENST00000509690.6:c.13_14delinsGA ENSP00000425104.2:p.Leu5Glu
ENST00000514944.6:c.130_131delinsGA ENSP00000423862.2:p.Leu44Glu
ENST00000604348.6:c.388_389delinsGA ENSP00000473895.2:p.Leu130Glu
ENST00000269305.9:c.409_410delinsGA MANE Select ENSP00000269305.4:p.Leu137Glu
ENST00000269305.8:c.409_410delinsGA ENSP00000269305.4:p.Leu137Glu
ENST00000359597.8:c.409_410delinsGA ENSP00000352610.4:p.Leu137Glu
ENST00000413465.6:c.409_410delinsGA ENSP00000410739.2:p.Leu137Glu
ENST00000420246.6:c.409_410delinsGA ENSP00000391127.2:p.Leu137Glu
ENST00000445888.6:c.409_410delinsGA ENSP00000391478.2:p.Leu137Glu
ENST00000455263.6:c.409_410delinsGA ENSP00000398846.2:p.Leu137Glu
ENST00000504290.5:c.13_14delinsGA ENSP00000484409.1:p.Leu5Glu
ENST00000504937.5:c.13_14delinsGA ENSP00000481179.1:p.Leu5Glu
ENST00000505014.5:n.665_666delinsGA
ENST00000508793.5:c.409_410delinsGA ENSP00000424104.1:p.Leu137Glu
ENST00000509690.5:c.13_14delinsGA ENSP00000425104.1:p.Leu5Glu
ENST00000510385.5:c.13_14delinsGA ENSP00000478499.1:p.Leu5Glu
ENST00000514944.5:c.130_131delinsGA ENSP00000423862.1:p.Leu44Glu
ENST00000604348.5:c.388_389delinsGA ENSP00000473895.1:p.Leu130Glu
ENST00000610292.4:c.292_293delinsGA ENSP00000478219.1:p.Leu98Glu
ENST00000610538.4:c.292_293delinsGA ENSP00000480868.1:p.Leu98Glu
ENST00000610623.4:c.-69_-68delinsGA ENSP00000477531.1:n.-69_-68delinsGA
ENST00000615910.4:c.376_377delinsGA ENSP00000482903.1:p.Leu126Glu
ENST00000617185.4:c.409_410delinsGA ENSP00000482258.1:p.Leu137Glu
ENST00000618944.4:c.-69_-68delinsGA ENSP00000481401.1:n.-69_-68delinsGA
ENST00000619186.4:c.-69_-68delinsGA ENSP00000484375.1:n.-69_-68delinsGA
ENST00000619485.4:c.292_293delinsGA ENSP00000482537.1:p.Leu98Glu
ENST00000620739.4:c.292_293delinsGA ENSP00000481638.1:p.Leu98Glu
ENST00000622645.4:c.292_293delinsGA ENSP00000482222.1:p.Leu98Glu
ENST00000635293.1:c.292_293delinsGA ENSP00000488924.1:p.Leu98Glu
NM_000546.5:c.409_410delinsGA , LRG_321t1:c.409_410delinsGA NP_000537.3:p.Leu137Glu
NM_001126112.2:c.409_410delinsGA , LRG_321t2:c.409_410delinsGA NP_001119584.1:p.Leu137Glu
NM_001126113.2:c.409_410delinsGA , LRG_321t4:c.409_410delinsGA NP_001119585.1:p.Leu137Glu
NM_001126114.2:c.409_410delinsGA , LRG_321t3:c.409_410delinsGA NP_001119586.1:p.Leu137Glu
NM_001126115.1:c.13_14delinsGA , LRG_321t5:c.13_14delinsGA NP_001119587.1:p.Leu5Glu
NM_001126116.1:c.13_14delinsGA , LRG_321t6:c.13_14delinsGA NP_001119588.1:p.Leu5Glu
NM_001126117.1:c.13_14delinsGA , LRG_321t7:c.13_14delinsGA NP_001119589.1:p.Leu5Glu
NM_001126118.1:c.292_293delinsGA , LRG_321t8:c.292_293delinsGA NP_001119590.1:p.Leu98Glu
NM_001276695.1:c.292_293delinsGA NP_001263624.1:p.Leu98Glu
NM_001276696.1:c.292_293delinsGA NP_001263625.1:p.Leu98Glu
NM_001276697.1:c.-69_-68delinsGA NP_001263626.1:n.-69_-68delinsGA
NM_001276698.1:c.-69_-68delinsGA NP_001263627.1:n.-69_-68delinsGA
NM_001276699.1:c.-69_-68delinsGA NP_001263628.1:n.-69_-68delinsGA
NM_001276760.1:c.292_293delinsGA NP_001263689.1:p.Leu98Glu
NM_001276761.1:c.292_293delinsGA NP_001263690.1:p.Leu98Glu
NM_001276695.2:c.292_293delinsGA NP_001263624.1:p.Leu98Glu
NM_001276696.2:c.292_293delinsGA NP_001263625.1:p.Leu98Glu
NM_001276697.2:c.-69_-68delinsGA NP_001263626.1:n.-69_-68delinsGA
NM_001276698.2:c.-69_-68delinsGA NP_001263627.1:n.-69_-68delinsGA
NM_001276699.2:c.-69_-68delinsGA NP_001263628.1:n.-69_-68delinsGA
NM_001276760.2:c.292_293delinsGA NP_001263689.1:p.Leu98Glu
NM_001276761.2:c.292_293delinsGA NP_001263690.1:p.Leu98Glu
NM_000546.6:c.409_410delinsGA MANE Select NP_000537.3:p.Leu137Glu
NM_001126112.3:c.409_410delinsGA NP_001119584.1:p.Leu137Glu
NM_001126113.3:c.409_410delinsGA NP_001119585.1:p.Leu137Glu
NM_001126114.3:c.409_410delinsGA NP_001119586.1:p.Leu137Glu
NM_001126115.2:c.13_14delinsGA NP_001119587.1:p.Leu5Glu
NM_001126116.2:c.13_14delinsGA NP_001119588.1:p.Leu5Glu
NM_001126117.2:c.13_14delinsGA NP_001119589.1:p.Leu5Glu
NM_001126118.2:c.292_293delinsGA NP_001119590.1:p.Leu98Glu
NM_001276695.3:c.292_293delinsGA NP_001263624.1:p.Leu98Glu
NM_001276696.3:c.292_293delinsGA NP_001263625.1:p.Leu98Glu
NM_001276697.3:c.-69_-68delinsGA NP_001263626.1:n.-69_-68delinsGA
NM_001276698.3:c.-69_-68delinsGA NP_001263627.1:n.-69_-68delinsGA
NM_001276699.3:c.-69_-68delinsGA NP_001263628.1:n.-69_-68delinsGA
NM_001276760.3:c.292_293delinsGA NP_001263689.1:p.Leu98Glu
NM_001276761.3:c.292_293delinsGA NP_001263690.1:p.Leu98Glu