Canonical Allele Identifier: CA397836936

Gene: TP53

Linked Data

• ClinVar Variation Id: 485044
• ClinVar RCV Id: RCV000561423 ; RCV000785448
• dbSNP Id: rs1555525279
• COSMIC: COSM43823 ; COSM5600710 ; COSM5600711 ; COSM5600712
• MyVariant Identifiers: chr17:g.7577113A>C (hg19) ; chr17:g.7673795A>C (hg38)
• PubMed: PMID:7887414 ; PMID:8023157 ; PMID:10567903 ; PMID:25584637

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7673795A>C , CM000679.2:g.7673795A>C	GRCh38
NC_000017.10:g.7577113A>C , CM000679.1:g.7577113A>C	GRCh37
NC_000017.9:g.7517838A>C	NCBI36
NG_017013.2:g.18756T>G , LRG_321:g.18756T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.825T>G	ENSP00000426252.2:p.Cys275Trp
ENST00000508793.6:c.825T>G	ENSP00000424104.2:p.Cys275Trp
ENST00000509690.6:c.429T>G	ENSP00000425104.2:p.Cys143Trp
ENST00000514944.6:c.546T>G	ENSP00000423862.2:p.Cys182Trp
ENST00000604348.6:c.804T>G	ENSP00000473895.2:p.Cys268Trp
ENST00000269305.9:c.825T>G MANE Select	ENSP00000269305.4:p.Cys275Trp
ENST00000269305.8:c.825T>G	ENSP00000269305.4:p.Cys275Trp
ENST00000359597.8:c.825T>G	ENSP00000352610.4:p.Cys275Trp
ENST00000413465.6:c.782+386T>G	ENSP00000410739.2:n.782+386T>G
ENST00000420246.6:c.825T>G	ENSP00000391127.2:p.Cys275Trp
ENST00000445888.6:c.825T>G	ENSP00000391478.2:p.Cys275Trp
ENST00000455263.6:c.825T>G	ENSP00000398846.2:p.Cys275Trp
ENST00000504290.5:c.429T>G	ENSP00000484409.1:p.Cys143Trp
ENST00000504937.5:c.429T>G	ENSP00000481179.1:p.Cys143Trp
ENST00000509690.5:c.429T>G	ENSP00000425104.1:p.Cys143Trp
ENST00000510385.5:c.429T>G	ENSP00000478499.1:p.Cys143Trp
ENST00000610292.4:c.708T>G	ENSP00000478219.1:p.Cys236Trp
ENST00000610538.4:c.708T>G	ENSP00000480868.1:p.Cys236Trp
ENST00000610623.4:c.348T>G	ENSP00000477531.1:p.Cys116Trp
ENST00000615910.4:c.792T>G	ENSP00000482903.1:p.Cys264Trp
ENST00000617185.4:c.825T>G	ENSP00000482258.1:p.Cys275Trp
ENST00000618944.4:c.348T>G	ENSP00000481401.1:p.Cys116Trp
ENST00000619186.4:c.348T>G	ENSP00000484375.1:p.Cys116Trp
ENST00000619485.4:c.708T>G	ENSP00000482537.1:p.Cys236Trp
ENST00000620739.4:c.708T>G	ENSP00000481638.1:p.Cys236Trp
ENST00000622645.4:c.708T>G	ENSP00000482222.1:p.Cys236Trp
ENST00000635293.1:c.708T>G	ENSP00000488924.1:p.Cys236Trp
NM_000546.5:c.825T>G , LRG_321t1:c.825T>G	NP_000537.3:p.Cys275Trp
NM_001126112.2:c.825T>G , LRG_321t2:c.825T>G	NP_001119584.1:p.Cys275Trp
NM_001126113.2:c.825T>G , LRG_321t4:c.825T>G	NP_001119585.1:p.Cys275Trp
NM_001126114.2:c.825T>G , LRG_321t3:c.825T>G	NP_001119586.1:p.Cys275Trp
NM_001126115.1:c.429T>G , LRG_321t5:c.429T>G	NP_001119587.1:p.Cys143Trp
NM_001126116.1:c.429T>G , LRG_321t6:c.429T>G	NP_001119588.1:p.Cys143Trp
NM_001126117.1:c.429T>G , LRG_321t7:c.429T>G	NP_001119589.1:p.Cys143Trp
NM_001126118.1:c.708T>G , LRG_321t8:c.708T>G	NP_001119590.1:p.Cys236Trp
NM_001276695.1:c.708T>G	NP_001263624.1:p.Cys236Trp
NM_001276696.1:c.708T>G	NP_001263625.1:p.Cys236Trp
NM_001276697.1:c.348T>G	NP_001263626.1:p.Cys116Trp
NM_001276698.1:c.348T>G	NP_001263627.1:p.Cys116Trp
NM_001276699.1:c.348T>G	NP_001263628.1:p.Cys116Trp
NM_001276760.1:c.708T>G	NP_001263689.1:p.Cys236Trp
NM_001276761.1:c.708T>G	NP_001263690.1:p.Cys236Trp
NM_001276695.2:c.708T>G	NP_001263624.1:p.Cys236Trp
NM_001276696.2:c.708T>G	NP_001263625.1:p.Cys236Trp
NM_001276697.2:c.348T>G	NP_001263626.1:p.Cys116Trp
NM_001276698.2:c.348T>G	NP_001263627.1:p.Cys116Trp
NM_001276699.2:c.348T>G	NP_001263628.1:p.Cys116Trp
NM_001276760.2:c.708T>G	NP_001263689.1:p.Cys236Trp
NM_001276761.2:c.708T>G	NP_001263690.1:p.Cys236Trp
NM_000546.6:c.825T>G MANE Select	NP_000537.3:p.Cys275Trp
NM_001126112.3:c.825T>G	NP_001119584.1:p.Cys275Trp
NM_001126113.3:c.825T>G	NP_001119585.1:p.Cys275Trp
NM_001126114.3:c.825T>G	NP_001119586.1:p.Cys275Trp
NM_001126115.2:c.429T>G	NP_001119587.1:p.Cys143Trp
NM_001126116.2:c.429T>G	NP_001119588.1:p.Cys143Trp
NM_001126117.2:c.429T>G	NP_001119589.1:p.Cys143Trp
NM_001126118.2:c.708T>G	NP_001119590.1:p.Cys236Trp
NM_001276695.3:c.708T>G	NP_001263624.1:p.Cys236Trp
NM_001276696.3:c.708T>G	NP_001263625.1:p.Cys236Trp
NM_001276697.3:c.348T>G	NP_001263626.1:p.Cys116Trp
NM_001276698.3:c.348T>G	NP_001263627.1:p.Cys116Trp
NM_001276699.3:c.348T>G	NP_001263628.1:p.Cys116Trp
NM_001276760.3:c.708T>G	NP_001263689.1:p.Cys236Trp
NM_001276761.3:c.708T>G	NP_001263690.1:p.Cys236Trp