Canonical Allele Identifier: CA645589135
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 824362
dbSNP Id: rs1597371154

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7675194_7675230del , CM000679.2:g.7675194_7675230del GRCh38
NC_000017.10:g.7578512_7578548del , CM000679.1:g.7578512_7578548del GRCh37
NC_000017.9:g.7519237_7519273del NCBI36
NG_017013.2:g.17329_17365del , LRG_321:g.17329_17365del

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.390_426del ENSP00000426252.2:p.Asn131CysfsTer27
ENST00000508793.6:c.390_426del ENSP00000424104.2:p.Asn131CysfsTer27
ENST00000509690.6:c.-7_30del
ENST00000514944.6:c.111_147del ENSP00000423862.2:p.Asn38CysfsTer27
ENST00000604348.6:c.376-7_405del
ENST00000269305.9:c.390_426del MANE Select ENSP00000269305.4:p.Asn131CysfsTer27
ENST00000269305.8:c.390_426del ENSP00000269305.4:p.Asn131CysfsTer27
ENST00000359597.8:c.390_426del ENSP00000352610.4:p.Asn131CysfsTer27
ENST00000413465.6:c.390_426del ENSP00000410739.2:p.Asn131CysfsTer27
ENST00000420246.6:c.390_426del ENSP00000391127.2:p.Asn131CysfsTer27
ENST00000445888.6:c.390_426del ENSP00000391478.2:p.Asn131CysfsTer27
ENST00000455263.6:c.390_426del ENSP00000398846.2:p.Asn131CysfsTer27
ENST00000504290.5:c.-7_30del
ENST00000504937.5:c.-7_30del
ENST00000505014.5:n.646_682del
ENST00000508793.5:c.390_426del ENSP00000424104.1:p.Asn131CysfsTer?
ENST00000509690.5:c.-7_30del
ENST00000510385.5:c.-7_30del
ENST00000514944.5:c.111_147del ENSP00000423862.1:p.Asn38CysfsTer27
ENST00000604348.5:c.376-7_405del
ENST00000610292.4:c.273_309del ENSP00000478219.1:p.Asn92CysfsTer27
ENST00000610538.4:c.273_309del ENSP00000480868.1:p.Asn92CysfsTer27
ENST00000610623.4:c.-88_-52del ENSP00000477531.1:n.-88_-52del
ENST00000615910.4:c.357_393del ENSP00000482903.1:p.Asn120CysfsTer27
ENST00000617185.4:c.390_426del ENSP00000482258.1:p.Asn131CysfsTer27
ENST00000618944.4:c.-88_-52del ENSP00000481401.1:n.-88_-52del
ENST00000619186.4:c.-88_-52del ENSP00000484375.1:n.-88_-52del
ENST00000619485.4:c.273_309del ENSP00000482537.1:p.Asn92CysfsTer27
ENST00000620739.4:c.273_309del ENSP00000481638.1:p.Asn92CysfsTer27
ENST00000622645.4:c.273_309del ENSP00000482222.1:p.Asn92CysfsTer27
ENST00000635293.1:c.273_309del ENSP00000488924.1:p.Asn92CysfsTer27
NM_000546.5:c.390_426del , LRG_321t1:c.390_426del NP_000537.3:p.Asn131CysfsTer27
NM_001126112.2:c.390_426del , LRG_321t2:c.390_426del NP_001119584.1:p.Asn131CysfsTer27
NM_001126113.2:c.390_426del , LRG_321t4:c.390_426del NP_001119585.1:p.Asn131CysfsTer27
NM_001126114.2:c.390_426del , LRG_321t3:c.390_426del NP_001119586.1:p.Asn131CysfsTer27
NM_001126115.1:c.-7_30del , LRG_321t5:c.-7_30del
NM_001126116.1:c.-7_30del , LRG_321t6:c.-7_30del
NM_001126117.1:c.-7_30del , LRG_321t7:c.-7_30del
NM_001126118.1:c.273_309del , LRG_321t8:c.273_309del NP_001119590.1:p.Asn92CysfsTer27
NM_001276695.1:c.273_309del NP_001263624.1:p.Asn92CysfsTer27
NM_001276696.1:c.273_309del NP_001263625.1:p.Asn92CysfsTer27
NM_001276697.1:c.-88_-52del NP_001263626.1:n.-88_-52del
NM_001276698.1:c.-88_-52del NP_001263627.1:n.-88_-52del
NM_001276699.1:c.-88_-52del NP_001263628.1:n.-88_-52del
NM_001276760.1:c.273_309del NP_001263689.1:p.Asn92CysfsTer27
NM_001276761.1:c.273_309del NP_001263690.1:p.Asn92CysfsTer27
NM_001276695.2:c.273_309del NP_001263624.1:p.Asn92CysfsTer27
NM_001276696.2:c.273_309del NP_001263625.1:p.Asn92CysfsTer27
NM_001276697.2:c.-88_-52del NP_001263626.1:n.-88_-52del
NM_001276698.2:c.-88_-52del NP_001263627.1:n.-88_-52del
NM_001276699.2:c.-88_-52del NP_001263628.1:n.-88_-52del
NM_001276760.2:c.273_309del NP_001263689.1:p.Asn92CysfsTer27
NM_001276761.2:c.273_309del NP_001263690.1:p.Asn92CysfsTer27
NM_000546.6:c.390_426del MANE Select NP_000537.3:p.Asn131CysfsTer27
NM_001126112.3:c.390_426del NP_001119584.1:p.Asn131CysfsTer27
NM_001126113.3:c.390_426del NP_001119585.1:p.Asn131CysfsTer27
NM_001126114.3:c.390_426del NP_001119586.1:p.Asn131CysfsTer27
NM_001126115.2:c.-7_30del
NM_001126116.2:c.-7_30del
NM_001126117.2:c.-7_30del
NM_001126118.2:c.273_309del NP_001119590.1:p.Asn92CysfsTer27
NM_001276695.3:c.273_309del NP_001263624.1:p.Asn92CysfsTer27
NM_001276696.3:c.273_309del NP_001263625.1:p.Asn92CysfsTer27
NM_001276697.3:c.-88_-52del NP_001263626.1:n.-88_-52del
NM_001276698.3:c.-88_-52del NP_001263627.1:n.-88_-52del
NM_001276699.3:c.-88_-52del NP_001263628.1:n.-88_-52del
NM_001276760.3:c.273_309del NP_001263689.1:p.Asn92CysfsTer27
NM_001276761.3:c.273_309del NP_001263690.1:p.Asn92CysfsTer27