Canonical Allele Identifier: CA000194

Gene: TP53

Linked Data

• ClinVar Variation Id: 133282
• ClinVar RCV Id: RCV000119795 ; RCV002514608
• dbSNP Id: rs137852790
• COSMIC: COSM43627 ; COSM5010328 ; COSM5010329 ; COSM5010330 ; COSM5010331 ; COSM5010332 ; COSM5010333
• MyVariant Identifiers: chr17:g.7578471_7578482del (hg19) ; chr17:g.7675153_7675164del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7675155_7675166del , CM000679.2:g.7675155_7675166del	GRCh38
NC_000017.10:g.7578473_7578484del , CM000679.1:g.7578473_7578484del	GRCh37
NC_000017.9:g.7519198_7519209del	NCBI36
NG_017013.2:g.17387_17398del , LRG_321:g.17387_17398del

Transcript Alleles

HGVS	Amino-acid change
ENST00000503591.2:c.448_459del	ENSP00000426252.2:p.Thr150_Pro153del
ENST00000508793.6:c.448_459del	ENSP00000424104.2:p.Thr150_Pro153del
ENST00000509690.6:c.52_63del	ENSP00000425104.2:p.Thr18_Pro21del
ENST00000514944.6:c.169_180del	ENSP00000423862.2:p.Thr57_Pro60del
ENST00000604348.6:c.427_438del	ENSP00000473895.2:p.Thr143_Pro146del
ENST00000269305.9:c.448_459del MANE Select	ENSP00000269305.4:p.Thr150_Pro153del
ENST00000269305.8:c.448_459del	ENSP00000269305.4:p.Thr150_Pro153del
ENST00000359597.8:c.448_459del	ENSP00000352610.4:p.Thr150_Pro153del
ENST00000413465.6:c.448_459del	ENSP00000410739.2:p.Thr150_Pro153del
ENST00000420246.6:c.448_459del	ENSP00000391127.2:p.Thr150_Pro153del
ENST00000445888.6:c.448_459del	ENSP00000391478.2:p.Thr150_Pro153del
ENST00000455263.6:c.448_459del	ENSP00000398846.2:p.Thr150_Pro153del
ENST00000504290.5:c.52_63del	ENSP00000484409.1:p.Thr18_Pro21del
ENST00000504937.5:c.52_63del	ENSP00000481179.1:p.Thr18_Pro21del
ENST00000505014.5:n.704_715del
ENST00000508793.5:c.448_459del	ENSP00000424104.1:p.Thr150_Pro153del
ENST00000509690.5:c.52_63del	ENSP00000425104.1:p.Thr18_Pro21del
ENST00000510385.5:c.52_63del	ENSP00000478499.1:p.Thr18_Pro21del
ENST00000514944.5:c.169_180del	ENSP00000423862.1:p.Thr57_Pro60del
ENST00000610292.4:c.331_342del	ENSP00000478219.1:p.Thr111_Pro114del
ENST00000610538.4:c.331_342del	ENSP00000480868.1:p.Thr111_Pro114del
ENST00000610623.4:c.-30_-19del	ENSP00000477531.1:n.-30_-19del
ENST00000615910.4:c.415_426del	ENSP00000482903.1:p.Thr139_Pro142del
ENST00000617185.4:c.448_459del	ENSP00000482258.1:p.Thr150_Pro153del
ENST00000618944.4:c.-30_-19del	ENSP00000481401.1:n.-30_-19del
ENST00000619186.4:c.-30_-19del	ENSP00000484375.1:n.-30_-19del
ENST00000619485.4:c.331_342del	ENSP00000482537.1:p.Thr111_Pro114del
ENST00000620739.4:c.331_342del	ENSP00000481638.1:p.Thr111_Pro114del
ENST00000622645.4:c.331_342del	ENSP00000482222.1:p.Thr111_Pro114del
ENST00000635293.1:c.331_342del	ENSP00000488924.1:p.Thr111_Pro114del
NM_000546.5:c.448_459del , LRG_321t1:c.448_459del	NP_000537.3:p.Thr150_Pro153del
NM_001126112.2:c.448_459del , LRG_321t2:c.448_459del	NP_001119584.1:p.Thr150_Pro153del
NM_001126113.2:c.448_459del , LRG_321t4:c.448_459del	NP_001119585.1:p.Thr150_Pro153del
NM_001126114.2:c.448_459del , LRG_321t3:c.448_459del	NP_001119586.1:p.Thr150_Pro153del
NM_001126115.1:c.52_63del , LRG_321t5:c.52_63del	NP_001119587.1:p.Thr18_Pro21del
NM_001126116.1:c.52_63del , LRG_321t6:c.52_63del	NP_001119588.1:p.Thr18_Pro21del
NM_001126117.1:c.52_63del , LRG_321t7:c.52_63del	NP_001119589.1:p.Thr18_Pro21del
NM_001126118.1:c.331_342del , LRG_321t8:c.331_342del	NP_001119590.1:p.Thr111_Pro114del
NM_001276695.1:c.331_342del	NP_001263624.1:p.Thr111_Pro114del
NM_001276696.1:c.331_342del	NP_001263625.1:p.Thr111_Pro114del
NM_001276697.1:c.-30_-19del	NP_001263626.1:n.-30_-19del
NM_001276698.1:c.-30_-19del	NP_001263627.1:n.-30_-19del
NM_001276699.1:c.-30_-19del	NP_001263628.1:n.-30_-19del
NM_001276760.1:c.331_342del	NP_001263689.1:p.Thr111_Pro114del
NM_001276761.1:c.331_342del	NP_001263690.1:p.Thr111_Pro114del
NM_001276695.2:c.331_342del	NP_001263624.1:p.Thr111_Pro114del
NM_001276696.2:c.331_342del	NP_001263625.1:p.Thr111_Pro114del
NM_001276697.2:c.-30_-19del	NP_001263626.1:n.-30_-19del
NM_001276698.2:c.-30_-19del	NP_001263627.1:n.-30_-19del
NM_001276699.2:c.-30_-19del	NP_001263628.1:n.-30_-19del
NM_001276760.2:c.331_342del	NP_001263689.1:p.Thr111_Pro114del
NM_001276761.2:c.331_342del	NP_001263690.1:p.Thr111_Pro114del
NM_000546.6:c.448_459del MANE Select	NP_000537.3:p.Thr150_Pro153del
NM_001126112.3:c.448_459del	NP_001119584.1:p.Thr150_Pro153del
NM_001126113.3:c.448_459del	NP_001119585.1:p.Thr150_Pro153del
NM_001126114.3:c.448_459del	NP_001119586.1:p.Thr150_Pro153del
NM_001126115.2:c.52_63del	NP_001119587.1:p.Thr18_Pro21del
NM_001126116.2:c.52_63del	NP_001119588.1:p.Thr18_Pro21del
NM_001126117.2:c.52_63del	NP_001119589.1:p.Thr18_Pro21del
NM_001126118.2:c.331_342del	NP_001119590.1:p.Thr111_Pro114del
NM_001276695.3:c.331_342del	NP_001263624.1:p.Thr111_Pro114del
NM_001276696.3:c.331_342del	NP_001263625.1:p.Thr111_Pro114del
NM_001276697.3:c.-30_-19del	NP_001263626.1:n.-30_-19del
NM_001276698.3:c.-30_-19del	NP_001263627.1:n.-30_-19del
NM_001276699.3:c.-30_-19del	NP_001263628.1:n.-30_-19del
NM_001276760.3:c.331_342del	NP_001263689.1:p.Thr111_Pro114del
NM_001276761.3:c.331_342del	NP_001263690.1:p.Thr111_Pro114del