Canonical Allele Identifier: CA2697552123

Gene: TP53

Linked Data

• ClinVar Variation Id: 2687652
• ClinVar RCV Id: RCV003484401

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7675225_7675226insT , CM000679.2:g.7675225_7675226insT	GRCh38
NC_000017.10:g.7578543_7578544insT , CM000679.1:g.7578543_7578544insT	GRCh37
NC_000017.9:g.7519268_7519269insT	NCBI36
NG_017013.2:g.17325_17326insA , LRG_321:g.17325_17326insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.386_387insA	ENSP00000426252.2:p.Leu130ProfsTer19
ENST00000508793.6:c.386_387insA	ENSP00000424104.2:p.Leu130ProfsTer19
ENST00000509690.6:c.-11_-10insA	ENSP00000425104.2:n.-11_-10insA
ENST00000514944.6:c.107_108insA	ENSP00000423862.2:p.Leu37ProfsTer19
ENST00000604348.6:c.376-11_376-10insA	ENSP00000473895.2:n.376-11_376-10insA
ENST00000269305.9:c.386_387insA MANE Select	ENSP00000269305.4:p.Leu130ProfsTer19
ENST00000269305.8:c.386_387insA	ENSP00000269305.4:p.Leu130ProfsTer19
ENST00000359597.8:c.386_387insA	ENSP00000352610.4:p.Leu130ProfsTer19
ENST00000413465.6:c.386_387insA	ENSP00000410739.2:p.Leu130ProfsTer19
ENST00000420246.6:c.386_387insA	ENSP00000391127.2:p.Leu130ProfsTer19
ENST00000445888.6:c.386_387insA	ENSP00000391478.2:p.Leu130ProfsTer19
ENST00000455263.6:c.386_387insA	ENSP00000398846.2:p.Leu130ProfsTer19
ENST00000504290.5:c.-11_-10insA	ENSP00000484409.1:n.-11_-10insA
ENST00000504937.5:c.-11_-10insA	ENSP00000481179.1:n.-11_-10insA
ENST00000505014.5:n.642_643insA
ENST00000508793.5:c.386_387insA	ENSP00000424104.1:p.Leu130ProfsTer19
ENST00000509690.5:c.-11_-10insA	ENSP00000425104.1:n.-11_-10insA
ENST00000510385.5:c.-11_-10insA	ENSP00000478499.1:n.-11_-10insA
ENST00000514944.5:c.107_108insA	ENSP00000423862.1:p.Leu37ProfsTer19
ENST00000604348.5:c.376-11_376-10insA	ENSP00000473895.1:n.376-11_376-10insA
ENST00000610292.4:c.269_270insA	ENSP00000478219.1:p.Leu91ProfsTer19
ENST00000610538.4:c.269_270insA	ENSP00000480868.1:p.Leu91ProfsTer19
ENST00000610623.4:c.-92_-91insA	ENSP00000477531.1:n.-92_-91insA
ENST00000615910.4:c.353_354insA	ENSP00000482903.1:p.Leu119ProfsTer19
ENST00000617185.4:c.386_387insA	ENSP00000482258.1:p.Leu130ProfsTer19
ENST00000618944.4:c.-92_-91insA	ENSP00000481401.1:n.-92_-91insA
ENST00000619186.4:c.-92_-91insA	ENSP00000484375.1:n.-92_-91insA
ENST00000619485.4:c.269_270insA	ENSP00000482537.1:p.Leu91ProfsTer19
ENST00000620739.4:c.269_270insA	ENSP00000481638.1:p.Leu91ProfsTer19
ENST00000622645.4:c.269_270insA	ENSP00000482222.1:p.Leu91ProfsTer19
ENST00000635293.1:c.269_270insA	ENSP00000488924.1:p.Leu91ProfsTer19
NM_000546.5:c.386_387insA , LRG_321t1:c.386_387insA	NP_000537.3:p.Leu130ProfsTer19
NM_001126112.2:c.386_387insA , LRG_321t2:c.386_387insA	NP_001119584.1:p.Leu130ProfsTer19
NM_001126113.2:c.386_387insA , LRG_321t4:c.386_387insA	NP_001119585.1:p.Leu130ProfsTer19
NM_001126114.2:c.386_387insA , LRG_321t3:c.386_387insA	NP_001119586.1:p.Leu130ProfsTer19
NM_001126115.1:c.-11_-10insA , LRG_321t5:c.-11_-10insA	NP_001119587.1:n.-11_-10insA
NM_001126116.1:c.-11_-10insA , LRG_321t6:c.-11_-10insA	NP_001119588.1:n.-11_-10insA
NM_001126117.1:c.-11_-10insA , LRG_321t7:c.-11_-10insA	NP_001119589.1:n.-11_-10insA
NM_001126118.1:c.269_270insA , LRG_321t8:c.269_270insA	NP_001119590.1:p.Leu91ProfsTer19
NM_001276695.1:c.269_270insA	NP_001263624.1:p.Leu91ProfsTer19
NM_001276696.1:c.269_270insA	NP_001263625.1:p.Leu91ProfsTer19
NM_001276697.1:c.-92_-91insA	NP_001263626.1:n.-92_-91insA
NM_001276698.1:c.-92_-91insA	NP_001263627.1:n.-92_-91insA
NM_001276699.1:c.-92_-91insA	NP_001263628.1:n.-92_-91insA
NM_001276760.1:c.269_270insA	NP_001263689.1:p.Leu91ProfsTer19
NM_001276761.1:c.269_270insA	NP_001263690.1:p.Leu91ProfsTer19
NM_001276695.2:c.269_270insA	NP_001263624.1:p.Leu91ProfsTer19
NM_001276696.2:c.269_270insA	NP_001263625.1:p.Leu91ProfsTer19
NM_001276697.2:c.-92_-91insA	NP_001263626.1:n.-92_-91insA
NM_001276698.2:c.-92_-91insA	NP_001263627.1:n.-92_-91insA
NM_001276699.2:c.-92_-91insA	NP_001263628.1:n.-92_-91insA
NM_001276760.2:c.269_270insA	NP_001263689.1:p.Leu91ProfsTer19
NM_001276761.2:c.269_270insA	NP_001263690.1:p.Leu91ProfsTer19
NM_000546.6:c.386_387insA MANE Select	NP_000537.3:p.Leu130ProfsTer19
NM_001126112.3:c.386_387insA	NP_001119584.1:p.Leu130ProfsTer19
NM_001126113.3:c.386_387insA	NP_001119585.1:p.Leu130ProfsTer19
NM_001126114.3:c.386_387insA	NP_001119586.1:p.Leu130ProfsTer19
NM_001126115.2:c.-11_-10insA	NP_001119587.1:n.-11_-10insA
NM_001126116.2:c.-11_-10insA	NP_001119588.1:n.-11_-10insA
NM_001126117.2:c.-11_-10insA	NP_001119589.1:n.-11_-10insA
NM_001126118.2:c.269_270insA	NP_001119590.1:p.Leu91ProfsTer19
NM_001276695.3:c.269_270insA	NP_001263624.1:p.Leu91ProfsTer19
NM_001276696.3:c.269_270insA	NP_001263625.1:p.Leu91ProfsTer19
NM_001276697.3:c.-92_-91insA	NP_001263626.1:n.-92_-91insA
NM_001276698.3:c.-92_-91insA	NP_001263627.1:n.-92_-91insA
NM_001276699.3:c.-92_-91insA	NP_001263628.1:n.-92_-91insA
NM_001276760.3:c.269_270insA	NP_001263689.1:p.Leu91ProfsTer19
NM_001276761.3:c.269_270insA	NP_001263690.1:p.Leu91ProfsTer19