Canonical Allele Identifier: CA2581463470
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7669609_7676594del , CM000679.2:g.7669609_7676594del GRCh38
NC_000017.10:g.7572927_7579912del , CM000679.1:g.7572927_7579912del GRCh37
NC_000017.9:g.7513652_7520637del NCBI36
NG_017013.2:g.15957_22942del , LRG_321:g.15957_22942del

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.1_1182del
ENST00000508793.6:c.1_1182del
ENST00000509690.6:c.-21-1358_786del
ENST00000514944.6:c.1_903del
ENST00000604348.6:c.1_1161del
ENST00000269305.9:c.1_1182del
ENST00000269305.8:c.1_1182del
ENST00000359597.8:c.1_994-3365del
ENST00000413465.6:c.1_782+4572del
ENST00000420246.6:c.1_*289del
ENST00000445888.6:c.1_1182del
ENST00000455263.6:c.1_*201del
ENST00000610292.4:c.-234_1065del
ENST00000610538.4:c.-117_*201del
ENST00000615910.4:c.1_1149del
ENST00000617185.4:c.1_*289del
ENST00000619485.4:c.-117_1065del
ENST00000620739.4:c.-117_1065del
ENST00000622645.4:c.-117_*289del
ENST00000635293.1:c.-117_983+1000del
NM_000546.5:c.1_1182del , LRG_321t1:c.1_1182del
NM_001126112.2:c.1_1182del , LRG_321t2:c.1_1182del
NM_001126113.2:c.1_*201del , LRG_321t4:c.1_*201del
NM_001126114.2:c.1_*289del , LRG_321t3:c.1_*289del
NM_001126118.1:c.-234_1065del , LRG_321t8:c.-234_1065del
NM_001276695.1:c.-117_*201del
NM_001276696.1:c.-117_*289del
NM_001276760.1:c.-117_1065del
NM_001276761.1:c.-117_1065del
NM_001276695.2:c.-117_*201del
NM_001276696.2:c.-117_*289del
NM_001276760.2:c.-117_1065del
NM_001276761.2:c.-117_1065del
NM_000546.6:c.1_1182del
NM_001126112.3:c.1_1182del
NM_001126113.3:c.1_*201del
NM_001126114.3:c.1_*289del
NM_001126118.2:c.-234_1065del
NM_001276695.3:c.-117_*201del
NM_001276696.3:c.-117_*289del
NM_001276760.3:c.-117_1065del
NM_001276761.3:c.-117_1065del