Canonical Allele Identifier: CA2850446912
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7669609_7674971del , CM000679.2:g.7669609_7674971del GRCh38
NC_000017.10:g.7572927_7578289del , CM000679.1:g.7572927_7578289del GRCh37
NC_000017.9:g.7513652_7519014del NCBI36
NG_017013.2:g.17580_22942del , LRG_321:g.17580_22942del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503591.2:c.560_1182del
ENST00000508793.6:c.560_1182del
ENST00000509690.6:c.164_786del
ENST00000514944.6:c.281_903del
ENST00000604348.6:c.539_1161del
ENST00000269305.9:c.560_1182del
ENST00000269305.8:c.560_1182del
ENST00000359597.8:c.560_994-3365del
ENST00000413465.6:c.560_782+4572del
ENST00000420246.6:c.560_*289del
ENST00000445888.6:c.560_1182del
ENST00000455263.6:c.560_*201del
ENST00000504290.5:c.164_*201del
ENST00000504937.5:c.164_786del
ENST00000510385.5:c.164_*289del
ENST00000610292.4:c.443_1065del
ENST00000610538.4:c.443_*201del
ENST00000610623.4:c.83_*201del
ENST00000615910.4:c.527_1149del
ENST00000617185.4:c.560_*289del
ENST00000618944.4:c.83_*289del
ENST00000619186.4:c.83_705del
ENST00000619485.4:c.443_1065del
ENST00000620739.4:c.443_1065del
ENST00000622645.4:c.443_*289del
ENST00000635293.1:c.443_983+1000del
NM_000546.5:c.560_1182del , LRG_321t1:c.560_1182del
NM_001126112.2:c.560_1182del , LRG_321t2:c.560_1182del
NM_001126113.2:c.560_*201del , LRG_321t4:c.560_*201del
NM_001126114.2:c.560_*289del , LRG_321t3:c.560_*289del
NM_001126115.1:c.164_786del , LRG_321t5:c.164_786del
NM_001126116.1:c.164_*289del , LRG_321t6:c.164_*289del
NM_001126117.1:c.164_*201del , LRG_321t7:c.164_*201del
NM_001126118.1:c.443_1065del , LRG_321t8:c.443_1065del
NM_001276695.1:c.443_*201del
NM_001276696.1:c.443_*289del
NM_001276697.1:c.83_705del
NM_001276698.1:c.83_*289del
NM_001276699.1:c.83_*201del
NM_001276760.1:c.443_1065del
NM_001276761.1:c.443_1065del
NM_001276695.2:c.443_*201del
NM_001276696.2:c.443_*289del
NM_001276697.2:c.83_705del
NM_001276698.2:c.83_*289del
NM_001276699.2:c.83_*201del
NM_001276760.2:c.443_1065del
NM_001276761.2:c.443_1065del
NM_000546.6:c.560_1182del
NM_001126112.3:c.560_1182del
NM_001126113.3:c.560_*201del
NM_001126114.3:c.560_*289del
NM_001126115.2:c.164_786del
NM_001126116.2:c.164_*289del
NM_001126117.2:c.164_*201del
NM_001126118.2:c.443_1065del
NM_001276695.3:c.443_*201del
NM_001276696.3:c.443_*289del
NM_001276697.3:c.83_705del
NM_001276698.3:c.83_*289del
NM_001276699.3:c.83_*201del
NM_001276760.3:c.443_1065del
NM_001276761.3:c.443_1065del