Canonical Allele Identifier: CA645589160
Gene: TP53 HGNC NCBI

Linked Data

COSMIC: COSM46362

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7675197_7676153del , CM000679.2:g.7675197_7676153del GRCh38
NC_000017.10:g.7578515_7579471del , CM000679.1:g.7578515_7579471del GRCh37
NC_000017.9:g.7519240_7520196del NCBI36
NG_017013.2:g.16398_17354del , LRG_321:g.16398_17354del

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.216_415del
ENST00000508793.6:c.216_415del
ENST00000509690.6:c.-21-917_19del
ENST00000514944.6:c.96+229_136del
ENST00000604348.6:c.216_394del
ENST00000269305.9:c.216_415del
ENST00000269305.8:c.216_415del
ENST00000359597.8:c.216_415del
ENST00000413465.6:c.216_415del
ENST00000420246.6:c.216_415del
ENST00000445888.6:c.216_415del
ENST00000455263.6:c.216_415del
ENST00000505014.5:n.472_671del
ENST00000508793.5:c.216_415del
ENST00000509690.5:c.-21-917_19del
ENST00000514944.5:c.96+229_136del
ENST00000604348.5:c.216_394del
ENST00000610292.4:c.99_298del
ENST00000610538.4:c.99_298del
ENST00000615910.4:c.216_382del
ENST00000617185.4:c.216_415del
ENST00000619485.4:c.99_298del
ENST00000620739.4:c.99_298del
ENST00000622645.4:c.99_298del
ENST00000635293.1:c.99_298del
NM_000546.5:c.216_415del , LRG_321t1:c.216_415del
NM_001126112.2:c.216_415del , LRG_321t2:c.216_415del
NM_001126113.2:c.216_415del , LRG_321t4:c.216_415del
NM_001126114.2:c.216_415del , LRG_321t3:c.216_415del
NM_001126118.1:c.99_298del , LRG_321t8:c.99_298del
NM_001276695.1:c.99_298del
NM_001276696.1:c.99_298del
NM_001276760.1:c.99_298del
NM_001276761.1:c.99_298del
NM_001276695.2:c.99_298del
NM_001276696.2:c.99_298del
NM_001276760.2:c.99_298del
NM_001276761.2:c.99_298del
NM_000546.6:c.216_415del
NM_001126112.3:c.216_415del
NM_001126113.3:c.216_415del
NM_001126114.3:c.216_415del
NM_001126118.2:c.99_298del
NM_001276695.3:c.99_298del
NM_001276696.3:c.99_298del
NM_001276760.3:c.99_298del
NM_001276761.3:c.99_298del