Canonical Allele Identifier: CA645587284
Gene: TP53 HGNC NCBI

Linked Data

COSMIC: COSM45756

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7669613_7669616del , CM000679.2:g.7669613_7669616del GRCh38
NC_000017.10:g.7572931_7572934del , CM000679.1:g.7572931_7572934del GRCh37
NC_000017.9:g.7513656_7513659del NCBI36
NG_017013.2:g.22936_22939del , LRG_321:g.22936_22939del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503591.2:c.1176_1179del ENSP00000426252.2:p.Ter394IleextTer27
ENST00000508793.6:c.1176_1179del ENSP00000424104.2:p.Ter394IleextTer27
ENST00000509690.6:c.780_783del ENSP00000425104.2:p.Ter262IleextTer27
ENST00000514944.6:c.897_900del ENSP00000423862.2:p.Ter301IleextTer27
ENST00000604348.6:c.1155_1158del ENSP00000473895.2:p.Ter387IleextTer27
ENST00000269305.9:c.1176_1179del MANE Select ENSP00000269305.4:p.Ter394IleextTer27
ENST00000269305.8:c.1176_1179del ENSP00000269305.4:p.Ter394IleextTer27
ENST00000359597.8:c.994-3371_994-3368del ENSP00000352610.4:n.994-3371_994-3368del
ENST00000413465.6:c.782+4566_782+4569del ENSP00000410739.2:n.782+4566_782+4569del
ENST00000420246.6:c.*283_*286del ENSP00000391127.2:n.*283_*286del
ENST00000445888.6:c.1176_1179del ENSP00000391478.2:p.Ter394IleextTer27
ENST00000455263.6:c.*195_*198del ENSP00000398846.2:n.*195_*198del
ENST00000504290.5:c.*195_*198del ENSP00000484409.1:n.*195_*198del
ENST00000504937.5:c.780_783del ENSP00000481179.1:p.Ter262IleextTer27
ENST00000510385.5:c.*283_*286del ENSP00000478499.1:n.*283_*286del
ENST00000576024.1:c.129_132del
ENST00000610292.4:c.1059_1062del ENSP00000478219.1:p.Ter355IleextTer27
ENST00000610538.4:c.*195_*198del ENSP00000480868.1:n.*195_*198del
ENST00000610623.4:c.*195_*198del ENSP00000477531.1:n.*195_*198del
ENST00000615910.4:c.1143_1146del ENSP00000482903.1:p.Ser381=
ENST00000617185.4:c.*283_*286del ENSP00000482258.1:n.*283_*286del
ENST00000618944.4:c.*283_*286del ENSP00000481401.1:n.*283_*286del
ENST00000619186.4:c.699_702del ENSP00000484375.1:p.Ter235IleextTer27
ENST00000619485.4:c.1059_1062del ENSP00000482537.1:p.Ter355IleextTer27
ENST00000620739.4:c.1059_1062del ENSP00000481638.1:p.Ter355IleextTer27
ENST00000622645.4:c.*283_*286del ENSP00000482222.1:n.*283_*286del
ENST00000635293.1:c.983+994_983+997del ENSP00000488924.1:n.983+994_983+997del
NM_000546.5:c.1176_1179del , LRG_321t1:c.1176_1179del NP_000537.3:p.Ter394IleextTer27
NM_001126112.2:c.1176_1179del , LRG_321t2:c.1176_1179del NP_001119584.1:p.Ter394IleextTer27
NM_001126113.2:c.*195_*198del , LRG_321t4:c.*195_*198del NP_001119585.1:n.*195_*198del
NM_001126114.2:c.*283_*286del , LRG_321t3:c.*283_*286del NP_001119586.1:n.*283_*286del
NM_001126115.1:c.780_783del , LRG_321t5:c.780_783del NP_001119587.1:p.Ter262IleextTer27
NM_001126116.1:c.*283_*286del , LRG_321t6:c.*283_*286del NP_001119588.1:n.*283_*286del
NM_001126117.1:c.*195_*198del , LRG_321t7:c.*195_*198del NP_001119589.1:n.*195_*198del
NM_001126118.1:c.1059_1062del , LRG_321t8:c.1059_1062del NP_001119590.1:p.Ter355IleextTer27
NM_001276695.1:c.*195_*198del NP_001263624.1:n.*195_*198del
NM_001276696.1:c.*283_*286del NP_001263625.1:n.*283_*286del
NM_001276697.1:c.699_702del NP_001263626.1:p.Ter235IleextTer27
NM_001276698.1:c.*283_*286del NP_001263627.1:n.*283_*286del
NM_001276699.1:c.*195_*198del NP_001263628.1:n.*195_*198del
NM_001276760.1:c.1059_1062del NP_001263689.1:p.Ter355IleextTer27
NM_001276761.1:c.1059_1062del NP_001263690.1:p.Ter355IleextTer27
NM_001276695.2:c.*195_*198del NP_001263624.1:n.*195_*198del
NM_001276696.2:c.*283_*286del NP_001263625.1:n.*283_*286del
NM_001276697.2:c.699_702del NP_001263626.1:p.Ter235IleextTer27
NM_001276698.2:c.*283_*286del NP_001263627.1:n.*283_*286del
NM_001276699.2:c.*195_*198del NP_001263628.1:n.*195_*198del
NM_001276760.2:c.1059_1062del NP_001263689.1:p.Ter355IleextTer27
NM_001276761.2:c.1059_1062del NP_001263690.1:p.Ter355IleextTer27
NM_000546.6:c.1176_1179del MANE Select NP_000537.3:p.Ter394IleextTer27
NM_001126112.3:c.1176_1179del NP_001119584.1:p.Ter394IleextTer27
NM_001126113.3:c.*195_*198del NP_001119585.1:n.*195_*198del
NM_001126114.3:c.*283_*286del NP_001119586.1:n.*283_*286del
NM_001126115.2:c.780_783del NP_001119587.1:p.Ter262IleextTer27
NM_001126116.2:c.*283_*286del NP_001119588.1:n.*283_*286del
NM_001126117.2:c.*195_*198del NP_001119589.1:n.*195_*198del
NM_001126118.2:c.1059_1062del NP_001119590.1:p.Ter355IleextTer27
NM_001276695.3:c.*195_*198del NP_001263624.1:n.*195_*198del
NM_001276696.3:c.*283_*286del NP_001263625.1:n.*283_*286del
NM_001276697.3:c.699_702del NP_001263626.1:p.Ter235IleextTer27
NM_001276698.3:c.*283_*286del NP_001263627.1:n.*283_*286del
NM_001276699.3:c.*195_*198del NP_001263628.1:n.*195_*198del
NM_001276760.3:c.1059_1062del NP_001263689.1:p.Ter355IleextTer27
NM_001276761.3:c.1059_1062del NP_001263690.1:p.Ter355IleextTer27