Canonical Allele Identifier: CA2838032356

Gene: TP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7670598_7670611del , CM000679.2:g.7670598_7670611del	GRCh38
NC_000017.10:g.7573916_7573929del , CM000679.1:g.7573916_7573929del	GRCh37
NC_000017.9:g.7514641_7514654del	NCBI36
NG_017013.2:g.21943_21956del , LRG_321:g.21943_21956del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.1100+1_1100+14del
ENST00000508793.6:c.1100+1_1100+14del
ENST00000509690.6:c.704+1_704+14del
ENST00000514944.6:c.821+1_821+14del
ENST00000604348.6:c.1079+1_1079+14del
ENST00000269305.9:c.1100+1_1100+14del
ENST00000269305.8:c.1100+1_1100+14del
ENST00000359597.8:c.993+2927_993+2940del	ENSP00000352610.4:n.993+2927_993+2940del
ENST00000413465.6:c.782+3573_782+3586del	ENSP00000410739.2:n.782+3573_782+3586del
ENST00000420246.6:c.*207+1_*207+14del
ENST00000445888.6:c.1100+1_1100+14del
ENST00000455263.6:c.*119+1_*119+14del
ENST00000504290.5:c.*119+1_*119+14del
ENST00000504937.5:c.704+1_704+14del
ENST00000510385.5:c.*207+1_*207+14del
ENST00000576024.1:c.54-918_54-905del
ENST00000610292.4:c.983+1_983+14del
ENST00000610538.4:c.*119+1_*119+14del
ENST00000610623.4:c.*119+1_*119+14del
ENST00000615910.4:c.1067+1_1067+14del
ENST00000617185.4:c.*207+1_*207+14del
ENST00000618944.4:c.*207+1_*207+14del
ENST00000619186.4:c.623+1_623+14del
ENST00000619485.4:c.983+1_983+14del
ENST00000620739.4:c.983+1_983+14del
ENST00000622645.4:c.*207+1_*207+14del
ENST00000635293.1:c.983+1_983+14del
NM_000546.5:c.1100+1_1100+14del , LRG_321t1:c.1100+1_1100+14del
NM_001126112.2:c.1100+1_1100+14del , LRG_321t2:c.1100+1_1100+14del
NM_001126113.2:c.*119+1_*119+14del , LRG_321t4:c.*119+1_*119+14del
NM_001126114.2:c.*207+1_*207+14del , LRG_321t3:c.*207+1_*207+14del
NM_001126115.1:c.704+1_704+14del , LRG_321t5:c.704+1_704+14del
NM_001126116.1:c.*207+1_*207+14del , LRG_321t6:c.*207+1_*207+14del
NM_001126117.1:c.*119+1_*119+14del , LRG_321t7:c.*119+1_*119+14del
NM_001126118.1:c.983+1_983+14del , LRG_321t8:c.983+1_983+14del
NM_001276695.1:c.*119+1_*119+14del
NM_001276696.1:c.*207+1_*207+14del
NM_001276697.1:c.623+1_623+14del
NM_001276698.1:c.*207+1_*207+14del
NM_001276699.1:c.*119+1_*119+14del
NM_001276760.1:c.983+1_983+14del
NM_001276761.1:c.983+1_983+14del
NM_001276695.2:c.*119+1_*119+14del
NM_001276696.2:c.*207+1_*207+14del
NM_001276697.2:c.623+1_623+14del
NM_001276698.2:c.*207+1_*207+14del
NM_001276699.2:c.*119+1_*119+14del
NM_001276760.2:c.983+1_983+14del
NM_001276761.2:c.983+1_983+14del
NM_000546.6:c.1100+1_1100+14del
NM_001126112.3:c.1100+1_1100+14del
NM_001126113.3:c.*119+1_*119+14del
NM_001126114.3:c.*207+1_*207+14del
NM_001126115.2:c.704+1_704+14del
NM_001126116.2:c.*207+1_*207+14del
NM_001126117.2:c.*119+1_*119+14del
NM_001126118.2:c.983+1_983+14del
NM_001276695.3:c.*119+1_*119+14del
NM_001276696.3:c.*207+1_*207+14del
NM_001276697.3:c.623+1_623+14del
NM_001276698.3:c.*207+1_*207+14del
NM_001276699.3:c.*119+1_*119+14del
NM_001276760.3:c.983+1_983+14del
NM_001276761.3:c.983+1_983+14del