Canonical Allele Identifier: CA891842270

Gene: TP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7675221_7675240del , CM000679.2:g.7675221_7675240del	GRCh38
NC_000017.10:g.7578539_7578558del , CM000679.1:g.7578539_7578558del	GRCh37
NC_000017.9:g.7519264_7519283del	NCBI36
NG_017013.2:g.17314_17333del , LRG_321:g.17314_17333del

Transcript Alleles

HGVS	Amino-acid change
ENST00000503591.2:c.376-1_394del
ENST00000508793.6:c.376-1_394del
ENST00000509690.6:c.-21-1_-3del
ENST00000514944.6:c.97-1_115del
ENST00000604348.6:c.376-22_376-3del	ENSP00000473895.2:n.376-22_376-3del
ENST00000269305.9:c.376-1_394del
ENST00000269305.8:c.376-1_394del
ENST00000359597.8:c.376-1_394del
ENST00000413465.6:c.376-1_394del
ENST00000420246.6:c.376-1_394del
ENST00000445888.6:c.376-1_394del
ENST00000455263.6:c.376-1_394del
ENST00000504290.5:c.-22_-3del	ENSP00000484409.1:n.-22_-3del
ENST00000504937.5:c.-22_-3del	ENSP00000481179.1:n.-22_-3del
ENST00000505014.5:n.632-1_650del
ENST00000508793.5:c.376-1_394del
ENST00000509690.5:c.-21-1_-3del
ENST00000510385.5:c.-22_-3del	ENSP00000478499.1:n.-22_-3del
ENST00000514944.5:c.97-1_115del
ENST00000604348.5:c.376-22_376-3del	ENSP00000473895.1:n.376-22_376-3del
ENST00000610292.4:c.259-1_277del
ENST00000610538.4:c.259-1_277del
ENST00000610623.4:c.-103_-84del	ENSP00000477531.1:n.-103_-84del
ENST00000615910.4:c.342_361del
ENST00000617185.4:c.376-1_394del
ENST00000618944.4:c.-103_-84del	ENSP00000481401.1:n.-103_-84del
ENST00000619186.4:c.-103_-84del	ENSP00000484375.1:n.-103_-84del
ENST00000619485.4:c.259-1_277del
ENST00000620739.4:c.259-1_277del
ENST00000622645.4:c.259-1_277del
ENST00000635293.1:c.259-1_277del
NM_000546.5:c.376-1_394del , LRG_321t1:c.376-1_394del
NM_001126112.2:c.376-1_394del , LRG_321t2:c.376-1_394del
NM_001126113.2:c.376-1_394del , LRG_321t4:c.376-1_394del
NM_001126114.2:c.376-1_394del , LRG_321t3:c.376-1_394del
NM_001126115.1:c.-22_-3del , LRG_321t5:c.-22_-3del	NP_001119587.1:n.-22_-3del
NM_001126116.1:c.-22_-3del , LRG_321t6:c.-22_-3del	NP_001119588.1:n.-22_-3del
NM_001126117.1:c.-22_-3del , LRG_321t7:c.-22_-3del	NP_001119589.1:n.-22_-3del
NM_001126118.1:c.259-1_277del , LRG_321t8:c.259-1_277del
NM_001276695.1:c.259-1_277del
NM_001276696.1:c.259-1_277del
NM_001276697.1:c.-103_-84del	NP_001263626.1:n.-103_-84del
NM_001276698.1:c.-103_-84del	NP_001263627.1:n.-103_-84del
NM_001276699.1:c.-103_-84del	NP_001263628.1:n.-103_-84del
NM_001276760.1:c.259-1_277del
NM_001276761.1:c.259-1_277del
NM_001276695.2:c.259-1_277del
NM_001276696.2:c.259-1_277del
NM_001276697.2:c.-103_-84del	NP_001263626.1:n.-103_-84del
NM_001276698.2:c.-103_-84del	NP_001263627.1:n.-103_-84del
NM_001276699.2:c.-103_-84del	NP_001263628.1:n.-103_-84del
NM_001276760.2:c.259-1_277del
NM_001276761.2:c.259-1_277del
NM_000546.6:c.376-1_394del
NM_001126112.3:c.376-1_394del
NM_001126113.3:c.376-1_394del
NM_001126114.3:c.376-1_394del
NM_001126115.2:c.-22_-3del	NP_001119587.1:n.-22_-3del
NM_001126116.2:c.-22_-3del	NP_001119588.1:n.-22_-3del
NM_001126117.2:c.-22_-3del	NP_001119589.1:n.-22_-3del
NM_001126118.2:c.259-1_277del
NM_001276695.3:c.259-1_277del
NM_001276696.3:c.259-1_277del
NM_001276697.3:c.-103_-84del	NP_001263626.1:n.-103_-84del
NM_001276698.3:c.-103_-84del	NP_001263627.1:n.-103_-84del
NM_001276699.3:c.-103_-84del	NP_001263628.1:n.-103_-84del
NM_001276760.3:c.259-1_277del
NM_001276761.3:c.259-1_277del