Canonical Allele Identifier: CA16615954
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406602
dbSNP Id: rs1064792930

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7675152_7675164del , CM000679.2:g.7675152_7675164del GRCh38
NC_000017.10:g.7578470_7578482del , CM000679.1:g.7578470_7578482del GRCh37
NC_000017.9:g.7519195_7519207del NCBI36
NG_017013.2:g.17387_17399del , LRG_321:g.17387_17399del

Transcript Alleles

HGVS Amino-acid change
ENST00000269305.8:c.448_460del ENSP00000269305.4:p.Thr150AlafsTer16
ENST00000359597.8:n.448_460del ENSP00000352610.4:p.Thr150AlafsTer16
ENST00000413465.6:n.448_460del ENSP00000410739.2:p.Thr150AlafsTer16
ENST00000420246.6:c.448_460del ENSP00000391127.2:p.Thr150AlafsTer16
ENST00000445888.6:c.448_460del ENSP00000391478.2:p.Thr150AlafsTer16
ENST00000455263.6:c.448_460del ENSP00000398846.2:p.Thr150AlafsTer16
ENST00000504290.5:c.52_64del ENSP00000484409.1:p.Thr18AlafsTer16
ENST00000504937.5:c.52_64del ENSP00000481179.1:p.Thr18AlafsTer16
ENST00000508793.5:c.448_460del ENSP00000424104.1:p.Thr150AlafsTer?
ENST00000509690.5:c.52_64del ENSP00000425104.1:p.Thr18AlafsTer16
ENST00000510385.5:c.52_64del ENSP00000478499.1:p.Thr18AlafsTer16
ENST00000514944.5:c.169_181del ENSP00000423862.1:p.Thr57AlafsTer16
ENST00000610292.4:c.331_343del ENSP00000478219.1:p.Thr111AlafsTer16
ENST00000610538.4:c.331_343del ENSP00000480868.1:p.Thr111AlafsTer16
ENST00000610623.4:c.-30_-18del ENSP00000477531.1:p.=
ENST00000615910.4:n.415_427del ENSP00000482903.1:p.Thr139AlafsTer16
ENST00000617185.4:c.448_460del ENSP00000482258.1:p.Thr150AlafsTer16
ENST00000618944.4:c.-30_-18del ENSP00000481401.1:p.=
ENST00000619186.4:c.-30_-18del ENSP00000484375.1:p.=
ENST00000619485.4:c.331_343del ENSP00000482537.1:p.Thr111AlafsTer16
ENST00000620739.4:c.331_343del ENSP00000481638.1:p.Thr111AlafsTer16
ENST00000622645.4:c.331_343del ENSP00000482222.1:p.Thr111AlafsTer16
ENST00000635293.1:c.331_343del ENSP00000488924.1:p.Thr111AlafsTer16
NM_000546.5:c.448_460del , LRG_321t1:c.448_460del NP_000537.3:p.Thr150AlafsTer16
NM_001126112.2:c.448_460del , LRG_321t2:c.448_460del NP_001119584.1:p.Thr150AlafsTer16
NM_001126113.2:c.448_460del , LRG_321t4:c.448_460del NP_001119585.1:p.Thr150AlafsTer16
NM_001126114.2:c.448_460del , LRG_321t3:c.448_460del NP_001119586.1:p.Thr150AlafsTer16
NM_001126115.1:c.52_64del , LRG_321t5:c.52_64del NP_001119587.1:p.Thr18AlafsTer16
NM_001126116.1:c.52_64del , LRG_321t6:c.52_64del NP_001119588.1:p.Thr18AlafsTer16
NM_001126117.1:c.52_64del , LRG_321t7:c.52_64del NP_001119589.1:p.Thr18AlafsTer16
NM_001126118.1:c.331_343del , LRG_321t8:c.331_343del NP_001119590.1:p.Thr111AlafsTer16
NM_001276695.1:c.331_343del NP_001263624.1:p.Thr111AlafsTer16
NM_001276696.1:c.331_343del NP_001263625.1:p.Thr111AlafsTer16
NM_001276697.1:c.-30_-18del NP_001263626.1:p.=
NM_001276698.1:c.-30_-18del NP_001263627.1:p.=
NM_001276699.1:c.-30_-18del NP_001263628.1:p.=
NM_001276760.1:c.331_343del NP_001263689.1:p.Thr111AlafsTer16
NM_001276761.1:c.331_343del NP_001263690.1:p.Thr111AlafsTer16
NM_001276695.2:c.331_343del NP_001263624.1:p.Thr111AlafsTer16
NM_001276696.2:c.331_343del NP_001263625.1:p.Thr111AlafsTer16
NM_001276697.2:c.-30_-18del NP_001263626.1:p.=
NM_001276698.2:c.-30_-18del NP_001263627.1:p.=
NM_001276699.2:c.-30_-18del NP_001263628.1:p.=
NM_001276760.2:c.331_343del NP_001263689.1:p.Thr111AlafsTer16
NM_001276761.2:c.331_343del NP_001263690.1:p.Thr111AlafsTer16
NM_000546.6:c.448_460del MANE Select NP_000537.3:p.Thr150AlafsTer16
NM_001126112.3:c.448_460del NP_001119584.1:p.Thr150AlafsTer16
NM_001126113.3:c.448_460del NP_001119585.1:p.Thr150AlafsTer16
NM_001126114.3:c.448_460del NP_001119586.1:p.Thr150AlafsTer16
NM_001126115.2:c.52_64del NP_001119587.1:p.Thr18AlafsTer16
NM_001126116.2:c.52_64del NP_001119588.1:p.Thr18AlafsTer16
NM_001126117.2:c.52_64del NP_001119589.1:p.Thr18AlafsTer16
NM_001126118.2:c.331_343del NP_001119590.1:p.Thr111AlafsTer16
NM_001276695.3:c.331_343del NP_001263624.1:p.Thr111AlafsTer16
NM_001276696.3:c.331_343del NP_001263625.1:p.Thr111AlafsTer16
NM_001276697.3:c.-30_-18del NP_001263626.1:p.=
NM_001276698.3:c.-30_-18del NP_001263627.1:p.=
NM_001276699.3:c.-30_-18del NP_001263628.1:p.=
NM_001276760.3:c.331_343del NP_001263689.1:p.Thr111AlafsTer16
NM_001276761.3:c.331_343del NP_001263690.1:p.Thr111AlafsTer16