Canonical Allele Identifier: CA16620639
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 418516
ClinVar RCV Id: RCV000486807
dbSNP Id: rs1064793279

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7676115del , CM000679.2:g.7676115del GRCh38
NC_000017.10:g.7579433del , CM000679.1:g.7579433del GRCh37
NC_000017.9:g.7520158del NCBI36
NG_017013.2:g.16433del , LRG_321:g.16433del

Transcript Alleles

HGVS Amino-acid change
ENST00000269305.8:c.251del ENSP00000269305.4:p.Pro85LeufsTer?
ENST00000359597.8:n.251del ENSP00000352610.4:p.Pro85LeufsTer?
ENST00000413465.6:n.251del ENSP00000410739.2:p.Pro85LeufsTer?
ENST00000420246.6:c.251del ENSP00000391127.2:p.Pro85LeufsTer?
ENST00000445888.6:c.251del ENSP00000391478.2:p.Pro85LeufsTer?
ENST00000455263.6:c.251del ENSP00000398846.2:p.Pro85LeufsTer?
ENST00000503591.1:c.251del ENSP00000426252.1:p.Pro85LeufsTer?
ENST00000508793.5:c.251del ENSP00000424104.1:p.Pro85LeufsTer?
ENST00000509690.5:c.-21-882del ENSP00000425104.1:p.=
ENST00000514944.5:c.96+264del ENSP00000423862.1:p.=
ENST00000604348.5:c.251del ENSP00000473895.1:p.Pro85LeufsTer?
ENST00000610292.4:c.134del ENSP00000478219.1:p.Pro46LeufsTer?
ENST00000610538.4:c.134del ENSP00000480868.1:p.Pro46LeufsTer?
ENST00000615910.4:n.251del ENSP00000482903.1:p.Pro85LeufsTer?
ENST00000617185.4:c.251del ENSP00000482258.1:p.Pro85LeufsTer?
ENST00000619485.4:c.134del ENSP00000482537.1:p.Pro46LeufsTer?
ENST00000620739.4:c.134del ENSP00000481638.1:p.Pro46LeufsTer?
ENST00000622645.4:c.134del ENSP00000482222.1:p.Pro46LeufsTer?
ENST00000635293.1:c.134del ENSP00000488924.1:p.Pro46LeufsTer?
NM_000546.5:c.251del , LRG_321t1:c.251del NP_000537.3:p.Pro85LeufsTer?
NM_001126112.2:c.251del , LRG_321t2:c.251del NP_001119584.1:p.Pro85LeufsTer?
NM_001126113.2:c.251del , LRG_321t4:c.251del NP_001119585.1:p.Pro85LeufsTer?
NM_001126114.2:c.251del , LRG_321t3:c.251del NP_001119586.1:p.Pro85LeufsTer?
NM_001126118.1:c.134del , LRG_321t8:c.134del NP_001119590.1:p.Pro46LeufsTer?
NM_001276695.1:c.134del NP_001263624.1:p.Pro46LeufsTer?
NM_001276696.1:c.134del NP_001263625.1:p.Pro46LeufsTer?
NM_001276760.1:c.134del NP_001263689.1:p.Pro46LeufsTer?
NM_001276761.1:c.134del NP_001263690.1:p.Pro46LeufsTer?
NM_001276695.2:c.134del NP_001263624.1:p.Pro46LeufsTer?
NM_001276696.2:c.134del NP_001263625.1:p.Pro46LeufsTer?
NM_001276760.2:c.134del NP_001263689.1:p.Pro46LeufsTer?
NM_001276761.2:c.134del NP_001263690.1:p.Pro46LeufsTer?
NM_000546.6:c.251del MANE Select NP_000537.3:p.Pro85LeufsTer?
NM_001126112.3:c.251del NP_001119584.1:p.Pro85LeufsTer?
NM_001126113.3:c.251del NP_001119585.1:p.Pro85LeufsTer?
NM_001126114.3:c.251del NP_001119586.1:p.Pro85LeufsTer?
NM_001126118.2:c.134del NP_001119590.1:p.Pro46LeufsTer?
NM_001276695.3:c.134del NP_001263624.1:p.Pro46LeufsTer?
NM_001276696.3:c.134del NP_001263625.1:p.Pro46LeufsTer?
NM_001276760.3:c.134del NP_001263689.1:p.Pro46LeufsTer?
NM_001276761.3:c.134del NP_001263690.1:p.Pro46LeufsTer?