Canonical Allele Identifier: CA397842769

Gene: TP53

Linked Data

• ClinVar Variation Id: 480751
• ClinVar RCV Id: RCV000572692 ; RCV001352113 ; RCV002289793
• dbSNP Id: rs1555526268
• COSMIC: COSM43767 ; COSM437597 ; COSM437598 ; COSM437599 ; COSM437600 ; COSM2153121 ; COSM3403290
• MyVariant Identifiers: chr17:g.7578524G>C (hg19) ; chr17:g.7675206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7675206G>C , CM000679.2:g.7675206G>C	GRCh38
NC_000017.10:g.7578524G>C , CM000679.1:g.7578524G>C	GRCh37
NC_000017.9:g.7519249G>C	NCBI36
NG_017013.2:g.17345C>G , LRG_321:g.17345C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.406C>G	ENSP00000426252.2:p.Gln136Glu
ENST00000508793.6:c.406C>G	ENSP00000424104.2:p.Gln136Glu
ENST00000509690.6:c.10C>G	ENSP00000425104.2:p.Gln4Glu
ENST00000514944.6:c.127C>G	ENSP00000423862.2:p.Gln43Glu
ENST00000604348.6:c.385C>G	ENSP00000473895.2:p.Gln129Glu
ENST00000269305.9:c.406C>G MANE Select	ENSP00000269305.4:p.Gln136Glu
ENST00000269305.8:c.406C>G	ENSP00000269305.4:p.Gln136Glu
ENST00000359597.8:c.406C>G	ENSP00000352610.4:p.Gln136Glu
ENST00000413465.6:c.406C>G	ENSP00000410739.2:p.Gln136Glu
ENST00000420246.6:c.406C>G	ENSP00000391127.2:p.Gln136Glu
ENST00000445888.6:c.406C>G	ENSP00000391478.2:p.Gln136Glu
ENST00000455263.6:c.406C>G	ENSP00000398846.2:p.Gln136Glu
ENST00000504290.5:c.10C>G	ENSP00000484409.1:p.Gln4Glu
ENST00000504937.5:c.10C>G	ENSP00000481179.1:p.Gln4Glu
ENST00000505014.5:n.662C>G
ENST00000508793.5:c.406C>G	ENSP00000424104.1:p.Gln136Glu
ENST00000509690.5:c.10C>G	ENSP00000425104.1:p.Gln4Glu
ENST00000510385.5:c.10C>G	ENSP00000478499.1:p.Gln4Glu
ENST00000514944.5:c.127C>G	ENSP00000423862.1:p.Gln43Glu
ENST00000604348.5:c.385C>G	ENSP00000473895.1:p.Gln129Glu
ENST00000610292.4:c.289C>G	ENSP00000478219.1:p.Gln97Glu
ENST00000610538.4:c.289C>G	ENSP00000480868.1:p.Gln97Glu
ENST00000610623.4:c.-72C>G	ENSP00000477531.1:n.-72C>G
ENST00000615910.4:c.373C>G	ENSP00000482903.1:p.Gln125Glu
ENST00000617185.4:c.406C>G	ENSP00000482258.1:p.Gln136Glu
ENST00000618944.4:c.-72C>G	ENSP00000481401.1:n.-72C>G
ENST00000619186.4:c.-72C>G	ENSP00000484375.1:n.-72C>G
ENST00000619485.4:c.289C>G	ENSP00000482537.1:p.Gln97Glu
ENST00000620739.4:c.289C>G	ENSP00000481638.1:p.Gln97Glu
ENST00000622645.4:c.289C>G	ENSP00000482222.1:p.Gln97Glu
ENST00000635293.1:c.289C>G	ENSP00000488924.1:p.Gln97Glu
NM_000546.5:c.406C>G , LRG_321t1:c.406C>G	NP_000537.3:p.Gln136Glu
NM_001126112.2:c.406C>G , LRG_321t2:c.406C>G	NP_001119584.1:p.Gln136Glu
NM_001126113.2:c.406C>G , LRG_321t4:c.406C>G	NP_001119585.1:p.Gln136Glu
NM_001126114.2:c.406C>G , LRG_321t3:c.406C>G	NP_001119586.1:p.Gln136Glu
NM_001126115.1:c.10C>G , LRG_321t5:c.10C>G	NP_001119587.1:p.Gln4Glu
NM_001126116.1:c.10C>G , LRG_321t6:c.10C>G	NP_001119588.1:p.Gln4Glu
NM_001126117.1:c.10C>G , LRG_321t7:c.10C>G	NP_001119589.1:p.Gln4Glu
NM_001126118.1:c.289C>G , LRG_321t8:c.289C>G	NP_001119590.1:p.Gln97Glu
NM_001276695.1:c.289C>G	NP_001263624.1:p.Gln97Glu
NM_001276696.1:c.289C>G	NP_001263625.1:p.Gln97Glu
NM_001276697.1:c.-72C>G	NP_001263626.1:n.-72C>G
NM_001276698.1:c.-72C>G	NP_001263627.1:n.-72C>G
NM_001276699.1:c.-72C>G	NP_001263628.1:n.-72C>G
NM_001276760.1:c.289C>G	NP_001263689.1:p.Gln97Glu
NM_001276761.1:c.289C>G	NP_001263690.1:p.Gln97Glu
NM_001276695.2:c.289C>G	NP_001263624.1:p.Gln97Glu
NM_001276696.2:c.289C>G	NP_001263625.1:p.Gln97Glu
NM_001276697.2:c.-72C>G	NP_001263626.1:n.-72C>G
NM_001276698.2:c.-72C>G	NP_001263627.1:n.-72C>G
NM_001276699.2:c.-72C>G	NP_001263628.1:n.-72C>G
NM_001276760.2:c.289C>G	NP_001263689.1:p.Gln97Glu
NM_001276761.2:c.289C>G	NP_001263690.1:p.Gln97Glu
NM_000546.6:c.406C>G MANE Select	NP_000537.3:p.Gln136Glu
NM_001126112.3:c.406C>G	NP_001119584.1:p.Gln136Glu
NM_001126113.3:c.406C>G	NP_001119585.1:p.Gln136Glu
NM_001126114.3:c.406C>G	NP_001119586.1:p.Gln136Glu
NM_001126115.2:c.10C>G	NP_001119587.1:p.Gln4Glu
NM_001126116.2:c.10C>G	NP_001119588.1:p.Gln4Glu
NM_001126117.2:c.10C>G	NP_001119589.1:p.Gln4Glu
NM_001126118.2:c.289C>G	NP_001119590.1:p.Gln97Glu
NM_001276695.3:c.289C>G	NP_001263624.1:p.Gln97Glu
NM_001276696.3:c.289C>G	NP_001263625.1:p.Gln97Glu
NM_001276697.3:c.-72C>G	NP_001263626.1:n.-72C>G
NM_001276698.3:c.-72C>G	NP_001263627.1:n.-72C>G
NM_001276699.3:c.-72C>G	NP_001263628.1:n.-72C>G
NM_001276760.3:c.289C>G	NP_001263689.1:p.Gln97Glu
NM_001276761.3:c.289C>G	NP_001263690.1:p.Gln97Glu