Canonical Allele Identifier: CA915949512
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 822031
ClinVar RCV Id: RCV001017048
dbSNP Id: rs1597349305

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7670684_7670685delinsAA , CM000679.2:g.7670684_7670685delinsAA GRCh38
NC_000017.10:g.7574002_7574003delinsAA , CM000679.1:g.7574002_7574003delinsAA GRCh37
NC_000017.9:g.7514727_7514728delinsAA NCBI36
NG_017013.2:g.21866_21867delinsTT , LRG_321:g.21866_21867delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000503591.2:c.1024_1025delinsTT ENSP00000426252.2:p.Arg342Leu
ENST00000508793.6:c.1024_1025delinsTT ENSP00000424104.2:p.Arg342Leu
ENST00000509690.6:c.628_629delinsTT ENSP00000425104.2:p.Arg210Leu
ENST00000514944.6:c.745_746delinsTT ENSP00000423862.2:p.Arg249Leu
ENST00000604348.6:c.1003_1004delinsTT ENSP00000473895.2:p.Arg335Leu
ENST00000269305.9:c.1024_1025delinsTT MANE Select ENSP00000269305.4:p.Arg342Leu
ENST00000269305.8:c.1024_1025delinsTT ENSP00000269305.4:p.Arg342Leu
ENST00000359597.8:c.993+2850_993+2851delinsTT ENSP00000352610.4:n.993+2850_993+2851delinsTT
ENST00000413465.6:c.782+3496_782+3497delinsTT ENSP00000410739.2:n.782+3496_782+3497delinsTT
ENST00000420246.6:c.*131_*132delinsTT ENSP00000391127.2:n.*131_*132delinsTT
ENST00000445888.6:c.1024_1025delinsTT ENSP00000391478.2:p.Arg342Leu
ENST00000455263.6:c.*43_*44delinsTT ENSP00000398846.2:n.*43_*44delinsTT
ENST00000504290.5:c.*43_*44delinsTT ENSP00000484409.1:n.*43_*44delinsTT
ENST00000504937.5:c.628_629delinsTT ENSP00000481179.1:p.Arg210Leu
ENST00000510385.5:c.*131_*132delinsTT ENSP00000478499.1:n.*131_*132delinsTT
ENST00000576024.1:c.54-995_54-994delinsTT
ENST00000610292.4:c.907_908delinsTT ENSP00000478219.1:p.Arg303Leu
ENST00000610538.4:c.*43_*44delinsTT ENSP00000480868.1:n.*43_*44delinsTT
ENST00000610623.4:c.*43_*44delinsTT ENSP00000477531.1:n.*43_*44delinsTT
ENST00000615910.4:c.991_992delinsTT ENSP00000482903.1:p.Arg331Leu
ENST00000617185.4:c.*131_*132delinsTT ENSP00000482258.1:n.*131_*132delinsTT
ENST00000618944.4:c.*131_*132delinsTT ENSP00000481401.1:n.*131_*132delinsTT
ENST00000619186.4:c.547_548delinsTT ENSP00000484375.1:p.Arg183Leu
ENST00000619485.4:c.907_908delinsTT ENSP00000482537.1:p.Arg303Leu
ENST00000620739.4:c.907_908delinsTT ENSP00000481638.1:p.Arg303Leu
ENST00000622645.4:c.*131_*132delinsTT ENSP00000482222.1:n.*131_*132delinsTT
ENST00000635293.1:c.907_908delinsTT ENSP00000488924.1:p.Arg303Leu
NM_000546.5:c.1024_1025delinsTT , LRG_321t1:c.1024_1025delinsTT NP_000537.3:p.Arg342Leu
NM_001126112.2:c.1024_1025delinsTT , LRG_321t2:c.1024_1025delinsTT NP_001119584.1:p.Arg342Leu
NM_001126113.2:c.*43_*44delinsTT , LRG_321t4:c.*43_*44delinsTT NP_001119585.1:n.*43_*44delinsTT
NM_001126114.2:c.*131_*132delinsTT , LRG_321t3:c.*131_*132delinsTT NP_001119586.1:n.*131_*132delinsTT
NM_001126115.1:c.628_629delinsTT , LRG_321t5:c.628_629delinsTT NP_001119587.1:p.Arg210Leu
NM_001126116.1:c.*131_*132delinsTT , LRG_321t6:c.*131_*132delinsTT NP_001119588.1:n.*131_*132delinsTT
NM_001126117.1:c.*43_*44delinsTT , LRG_321t7:c.*43_*44delinsTT NP_001119589.1:n.*43_*44delinsTT
NM_001126118.1:c.907_908delinsTT , LRG_321t8:c.907_908delinsTT NP_001119590.1:p.Arg303Leu
NM_001276695.1:c.*43_*44delinsTT NP_001263624.1:n.*43_*44delinsTT
NM_001276696.1:c.*131_*132delinsTT NP_001263625.1:n.*131_*132delinsTT
NM_001276697.1:c.547_548delinsTT NP_001263626.1:p.Arg183Leu
NM_001276698.1:c.*131_*132delinsTT NP_001263627.1:n.*131_*132delinsTT
NM_001276699.1:c.*43_*44delinsTT NP_001263628.1:n.*43_*44delinsTT
NM_001276760.1:c.907_908delinsTT NP_001263689.1:p.Arg303Leu
NM_001276761.1:c.907_908delinsTT NP_001263690.1:p.Arg303Leu
NM_001276695.2:c.*43_*44delinsTT NP_001263624.1:n.*43_*44delinsTT
NM_001276696.2:c.*131_*132delinsTT NP_001263625.1:n.*131_*132delinsTT
NM_001276697.2:c.547_548delinsTT NP_001263626.1:p.Arg183Leu
NM_001276698.2:c.*131_*132delinsTT NP_001263627.1:n.*131_*132delinsTT
NM_001276699.2:c.*43_*44delinsTT NP_001263628.1:n.*43_*44delinsTT
NM_001276760.2:c.907_908delinsTT NP_001263689.1:p.Arg303Leu
NM_001276761.2:c.907_908delinsTT NP_001263690.1:p.Arg303Leu
NM_000546.6:c.1024_1025delinsTT MANE Select NP_000537.3:p.Arg342Leu
NM_001126112.3:c.1024_1025delinsTT NP_001119584.1:p.Arg342Leu
NM_001126113.3:c.*43_*44delinsTT NP_001119585.1:n.*43_*44delinsTT
NM_001126114.3:c.*131_*132delinsTT NP_001119586.1:n.*131_*132delinsTT
NM_001126115.2:c.628_629delinsTT NP_001119587.1:p.Arg210Leu
NM_001126116.2:c.*131_*132delinsTT NP_001119588.1:n.*131_*132delinsTT
NM_001126117.2:c.*43_*44delinsTT NP_001119589.1:n.*43_*44delinsTT
NM_001126118.2:c.907_908delinsTT NP_001119590.1:p.Arg303Leu
NM_001276695.3:c.*43_*44delinsTT NP_001263624.1:n.*43_*44delinsTT
NM_001276696.3:c.*131_*132delinsTT NP_001263625.1:n.*131_*132delinsTT
NM_001276697.3:c.547_548delinsTT NP_001263626.1:p.Arg183Leu
NM_001276698.3:c.*131_*132delinsTT NP_001263627.1:n.*131_*132delinsTT
NM_001276699.3:c.*43_*44delinsTT NP_001263628.1:n.*43_*44delinsTT
NM_001276760.3:c.907_908delinsTT NP_001263689.1:p.Arg303Leu
NM_001276761.3:c.907_908delinsTT NP_001263690.1:p.Arg303Leu