Canonical Allele Identifier: CA2245946913
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7673335_7673336delinsTG , CM000679.2:g.7673335_7673336delinsTG GRCh38
NC_000017.10:g.7576653_7576654delinsTG , CM000679.1:g.7576653_7576654delinsTG GRCh37
NC_000017.9:g.7517378_7517379delinsTG NCBI36
NG_017013.2:g.19215_19216delinsCA , LRG_321:g.19215_19216delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000503591.2:c.993+199_993+200delinsCA ENSP00000426252.2:n.993+199_993+200delinsCA
ENST00000508793.6:c.993+199_993+200delinsCA ENSP00000424104.2:n.993+199_993+200delinsCA
ENST00000509690.6:c.597+199_597+200delinsCA ENSP00000425104.2:n.597+199_597+200delinsCA
ENST00000514944.6:c.714+199_714+200delinsCA ENSP00000423862.2:n.714+199_714+200delinsCA
ENST00000604348.6:c.972+199_972+200delinsCA ENSP00000473895.2:n.972+199_972+200delinsCA
ENST00000269305.9:c.993+199_993+200delinsCA MANE Select ENSP00000269305.4:n.993+199_993+200delinsCA
ENST00000269305.8:c.993+199_993+200delinsCA ENSP00000269305.4:n.993+199_993+200delinsCA
ENST00000359597.8:c.993+199_993+200delinsCA ENSP00000352610.4:n.993+199_993+200delinsCA
ENST00000413465.6:c.782+845_782+846delinsCA ENSP00000410739.2:n.782+845_782+846delinsCA
ENST00000420246.6:c.997_998delinsCA ENSP00000391127.2:p.Gln333=
ENST00000445888.6:c.993+199_993+200delinsCA ENSP00000391478.2:n.993+199_993+200delinsCA
ENST00000455263.6:c.994-70_994-69delinsCA ENSP00000398846.2:n.994-70_994-69delinsCA
ENST00000504290.5:c.598-70_598-69delinsCA ENSP00000484409.1:n.598-70_598-69delinsCA
ENST00000504937.5:c.597+199_597+200delinsCA ENSP00000481179.1:n.597+199_597+200delinsCA
ENST00000510385.5:c.601_602delinsCA ENSP00000478499.1:p.Gln201=
ENST00000576024.1:c.53+199_53+200delinsCA
ENST00000610292.4:c.876+199_876+200delinsCA ENSP00000478219.1:n.876+199_876+200delinsCA
ENST00000610538.4:c.877-70_877-69delinsCA ENSP00000480868.1:n.877-70_877-69delinsCA
ENST00000610623.4:c.517-70_517-69delinsCA ENSP00000477531.1:n.517-70_517-69delinsCA
ENST00000615910.4:c.960+199_960+200delinsCA ENSP00000482903.1:n.960+199_960+200delinsCA
ENST00000617185.4:c.997_998delinsCA ENSP00000482258.1:p.Gln333=
ENST00000618944.4:c.520_521delinsCA ENSP00000481401.1:p.Gln174=
ENST00000619186.4:c.516+199_516+200delinsCA ENSP00000484375.1:n.516+199_516+200delinsCA
ENST00000619485.4:c.876+199_876+200delinsCA ENSP00000482537.1:n.876+199_876+200delinsCA
ENST00000620739.4:c.876+199_876+200delinsCA ENSP00000481638.1:n.876+199_876+200delinsCA
ENST00000622645.4:c.880_881delinsCA ENSP00000482222.1:p.Gln294=
ENST00000635293.1:c.876+199_876+200delinsCA ENSP00000488924.1:n.876+199_876+200delinsCA
NM_000546.5:c.993+199_993+200delinsCA , LRG_321t1:c.993+199_993+200delinsCA NP_000537.3:n.993+199_993+200delinsCA
NM_001126112.2:c.993+199_993+200delinsCA , LRG_321t2:c.993+199_993+200delinsCA NP_001119584.1:n.993+199_993+200delinsCA
NM_001126113.2:c.994-70_994-69delinsCA , LRG_321t4:c.994-70_994-69delinsCA NP_001119585.1:n.994-70_994-69delinsCA
NM_001126114.2:c.997_998delinsCA , LRG_321t3:c.997_998delinsCA NP_001119586.1:p.Gln333=
NM_001126115.1:c.597+199_597+200delinsCA , LRG_321t5:c.597+199_597+200delinsCA NP_001119587.1:n.597+199_597+200delinsCA
NM_001126116.1:c.601_602delinsCA , LRG_321t6:c.601_602delinsCA NP_001119588.1:p.Gln201=
NM_001126117.1:c.598-70_598-69delinsCA , LRG_321t7:c.598-70_598-69delinsCA NP_001119589.1:n.598-70_598-69delinsCA
NM_001126118.1:c.876+199_876+200delinsCA , LRG_321t8:c.876+199_876+200delinsCA NP_001119590.1:n.876+199_876+200delinsCA
NM_001276695.1:c.877-70_877-69delinsCA NP_001263624.1:n.877-70_877-69delinsCA
NM_001276696.1:c.880_881delinsCA NP_001263625.1:p.Gln294=
NM_001276697.1:c.516+199_516+200delinsCA NP_001263626.1:n.516+199_516+200delinsCA
NM_001276698.1:c.520_521delinsCA NP_001263627.1:p.Gln174=
NM_001276699.1:c.517-70_517-69delinsCA NP_001263628.1:n.517-70_517-69delinsCA
NM_001276760.1:c.876+199_876+200delinsCA NP_001263689.1:n.876+199_876+200delinsCA
NM_001276761.1:c.876+199_876+200delinsCA NP_001263690.1:n.876+199_876+200delinsCA
NM_001276695.2:c.877-70_877-69delinsCA NP_001263624.1:n.877-70_877-69delinsCA
NM_001276696.2:c.880_881delinsCA NP_001263625.1:p.Gln294=
NM_001276697.2:c.516+199_516+200delinsCA NP_001263626.1:n.516+199_516+200delinsCA
NM_001276698.2:c.520_521delinsCA NP_001263627.1:p.Gln174=
NM_001276699.2:c.517-70_517-69delinsCA NP_001263628.1:n.517-70_517-69delinsCA
NM_001276760.2:c.876+199_876+200delinsCA NP_001263689.1:n.876+199_876+200delinsCA
NM_001276761.2:c.876+199_876+200delinsCA NP_001263690.1:n.876+199_876+200delinsCA
NM_000546.6:c.993+199_993+200delinsCA MANE Select NP_000537.3:n.993+199_993+200delinsCA
NM_001126112.3:c.993+199_993+200delinsCA NP_001119584.1:n.993+199_993+200delinsCA
NM_001126113.3:c.994-70_994-69delinsCA NP_001119585.1:n.994-70_994-69delinsCA
NM_001126114.3:c.997_998delinsCA NP_001119586.1:p.Gln333=
NM_001126115.2:c.597+199_597+200delinsCA NP_001119587.1:n.597+199_597+200delinsCA
NM_001126116.2:c.601_602delinsCA NP_001119588.1:p.Gln201=
NM_001126117.2:c.598-70_598-69delinsCA NP_001119589.1:n.598-70_598-69delinsCA
NM_001126118.2:c.876+199_876+200delinsCA NP_001119590.1:n.876+199_876+200delinsCA
NM_001276695.3:c.877-70_877-69delinsCA NP_001263624.1:n.877-70_877-69delinsCA
NM_001276696.3:c.880_881delinsCA NP_001263625.1:p.Gln294=
NM_001276697.3:c.516+199_516+200delinsCA NP_001263626.1:n.516+199_516+200delinsCA
NM_001276698.3:c.520_521delinsCA NP_001263627.1:p.Gln174=
NM_001276699.3:c.517-70_517-69delinsCA NP_001263628.1:n.517-70_517-69delinsCA
NM_001276760.3:c.876+199_876+200delinsCA NP_001263689.1:n.876+199_876+200delinsCA
NM_001276761.3:c.876+199_876+200delinsCA NP_001263690.1:n.876+199_876+200delinsCA