Canonical Allele Identifier: CA2838032357
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7670683_7670687del , CM000679.2:g.7670683_7670687del GRCh38
NC_000017.10:g.7574001_7574005del , CM000679.1:g.7574001_7574005del GRCh37
NC_000017.9:g.7514726_7514730del NCBI36
NG_017013.2:g.21864_21868del , LRG_321:g.21864_21868del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503591.2:c.1022_1026del ENSP00000426252.2:p.Phe341Ter
ENST00000508793.6:c.1022_1026del ENSP00000424104.2:p.Phe341Ter
ENST00000509690.6:c.626_630del ENSP00000425104.2:p.Phe209Ter
ENST00000514944.6:c.743_747del ENSP00000423862.2:p.Phe248Ter
ENST00000604348.6:c.1001_1005del ENSP00000473895.2:p.Phe334Ter
ENST00000269305.9:c.1022_1026del MANE Select ENSP00000269305.4:p.Phe341Ter
ENST00000269305.8:c.1022_1026del ENSP00000269305.4:p.Phe341Ter
ENST00000359597.8:c.993+2848_993+2852del ENSP00000352610.4:n.993+2848_993+2852del
ENST00000413465.6:c.782+3494_782+3498del ENSP00000410739.2:n.782+3494_782+3498del
ENST00000420246.6:c.*129_*133del ENSP00000391127.2:n.*129_*133del
ENST00000445888.6:c.1022_1026del ENSP00000391478.2:p.Phe341Ter
ENST00000455263.6:c.*41_*45del ENSP00000398846.2:n.*41_*45del
ENST00000504290.5:c.*41_*45del ENSP00000484409.1:n.*41_*45del
ENST00000504937.5:c.626_630del ENSP00000481179.1:p.Phe209Ter
ENST00000510385.5:c.*129_*133del ENSP00000478499.1:n.*129_*133del
ENST00000576024.1:c.54-997_54-993del
ENST00000610292.4:c.905_909del ENSP00000478219.1:p.Phe302Ter
ENST00000610538.4:c.*41_*45del ENSP00000480868.1:n.*41_*45del
ENST00000610623.4:c.*41_*45del ENSP00000477531.1:n.*41_*45del
ENST00000615910.4:c.989_993del ENSP00000482903.1:p.Phe330Ter
ENST00000617185.4:c.*129_*133del ENSP00000482258.1:n.*129_*133del
ENST00000618944.4:c.*129_*133del ENSP00000481401.1:n.*129_*133del
ENST00000619186.4:c.545_549del ENSP00000484375.1:p.Phe182Ter
ENST00000619485.4:c.905_909del ENSP00000482537.1:p.Phe302Ter
ENST00000620739.4:c.905_909del ENSP00000481638.1:p.Phe302Ter
ENST00000622645.4:c.*129_*133del ENSP00000482222.1:n.*129_*133del
ENST00000635293.1:c.905_909del ENSP00000488924.1:p.Phe302Ter
NM_000546.5:c.1022_1026del , LRG_321t1:c.1022_1026del NP_000537.3:p.Phe341Ter
NM_001126112.2:c.1022_1026del , LRG_321t2:c.1022_1026del NP_001119584.1:p.Phe341Ter
NM_001126113.2:c.*41_*45del , LRG_321t4:c.*41_*45del NP_001119585.1:n.*41_*45del
NM_001126114.2:c.*129_*133del , LRG_321t3:c.*129_*133del NP_001119586.1:n.*129_*133del
NM_001126115.1:c.626_630del , LRG_321t5:c.626_630del NP_001119587.1:p.Phe209Ter
NM_001126116.1:c.*129_*133del , LRG_321t6:c.*129_*133del NP_001119588.1:n.*129_*133del
NM_001126117.1:c.*41_*45del , LRG_321t7:c.*41_*45del NP_001119589.1:n.*41_*45del
NM_001126118.1:c.905_909del , LRG_321t8:c.905_909del NP_001119590.1:p.Phe302Ter
NM_001276695.1:c.*41_*45del NP_001263624.1:n.*41_*45del
NM_001276696.1:c.*129_*133del NP_001263625.1:n.*129_*133del
NM_001276697.1:c.545_549del NP_001263626.1:p.Phe182Ter
NM_001276698.1:c.*129_*133del NP_001263627.1:n.*129_*133del
NM_001276699.1:c.*41_*45del NP_001263628.1:n.*41_*45del
NM_001276760.1:c.905_909del NP_001263689.1:p.Phe302Ter
NM_001276761.1:c.905_909del NP_001263690.1:p.Phe302Ter
NM_001276695.2:c.*41_*45del NP_001263624.1:n.*41_*45del
NM_001276696.2:c.*129_*133del NP_001263625.1:n.*129_*133del
NM_001276697.2:c.545_549del NP_001263626.1:p.Phe182Ter
NM_001276698.2:c.*129_*133del NP_001263627.1:n.*129_*133del
NM_001276699.2:c.*41_*45del NP_001263628.1:n.*41_*45del
NM_001276760.2:c.905_909del NP_001263689.1:p.Phe302Ter
NM_001276761.2:c.905_909del NP_001263690.1:p.Phe302Ter
NM_000546.6:c.1022_1026del MANE Select NP_000537.3:p.Phe341Ter
NM_001126112.3:c.1022_1026del NP_001119584.1:p.Phe341Ter
NM_001126113.3:c.*41_*45del NP_001119585.1:n.*41_*45del
NM_001126114.3:c.*129_*133del NP_001119586.1:n.*129_*133del
NM_001126115.2:c.626_630del NP_001119587.1:p.Phe209Ter
NM_001126116.2:c.*129_*133del NP_001119588.1:n.*129_*133del
NM_001126117.2:c.*41_*45del NP_001119589.1:n.*41_*45del
NM_001126118.2:c.905_909del NP_001119590.1:p.Phe302Ter
NM_001276695.3:c.*41_*45del NP_001263624.1:n.*41_*45del
NM_001276696.3:c.*129_*133del NP_001263625.1:n.*129_*133del
NM_001276697.3:c.545_549del NP_001263626.1:p.Phe182Ter
NM_001276698.3:c.*129_*133del NP_001263627.1:n.*129_*133del
NM_001276699.3:c.*41_*45del NP_001263628.1:n.*41_*45del
NM_001276760.3:c.905_909del NP_001263689.1:p.Phe302Ter
NM_001276761.3:c.905_909del NP_001263690.1:p.Phe302Ter