Canonical Allele Identifier: CA397837142

Gene: TP53

Linked Data

• ClinVar Variation Id: 458566
• ClinVar RCV Id: RCV000528667 ; RCV000785497 ; RCV001027016 ; RCV002289744
• dbSNP Id: rs1057519990
• COSMIC: COSM10794 ; COSM1559475 ; COSM1645293 ; COSM3388175
• MyVariant Identifiers: chr17:g.7577142C>T (hg19) ; chr17:g.7673824C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7673824C>T , CM000679.2:g.7673824C>T	GRCh38
NC_000017.10:g.7577142C>T , CM000679.1:g.7577142C>T	GRCh37
NC_000017.9:g.7517867C>T	NCBI36
NG_017013.2:g.18727G>A , LRG_321:g.18727G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.796G>A	ENSP00000426252.2:p.Gly266Arg
ENST00000508793.6:c.796G>A	ENSP00000424104.2:p.Gly266Arg
ENST00000509690.6:c.400G>A	ENSP00000425104.2:p.Gly134Arg
ENST00000514944.6:c.517G>A	ENSP00000423862.2:p.Gly173Arg
ENST00000604348.6:c.775G>A	ENSP00000473895.2:p.Gly259Arg
ENST00000269305.9:c.796G>A MANE Select	ENSP00000269305.4:p.Gly266Arg
ENST00000269305.8:c.796G>A	ENSP00000269305.4:p.Gly266Arg
ENST00000359597.8:c.796G>A	ENSP00000352610.4:p.Gly266Arg
ENST00000413465.6:c.782+357G>A	ENSP00000410739.2:n.782+357G>A
ENST00000420246.6:c.796G>A	ENSP00000391127.2:p.Gly266Arg
ENST00000445888.6:c.796G>A	ENSP00000391478.2:p.Gly266Arg
ENST00000455263.6:c.796G>A	ENSP00000398846.2:p.Gly266Arg
ENST00000504290.5:c.400G>A	ENSP00000484409.1:p.Gly134Arg
ENST00000504937.5:c.400G>A	ENSP00000481179.1:p.Gly134Arg
ENST00000509690.5:c.400G>A	ENSP00000425104.1:p.Gly134Arg
ENST00000510385.5:c.400G>A	ENSP00000478499.1:p.Gly134Arg
ENST00000610292.4:c.679G>A	ENSP00000478219.1:p.Gly227Arg
ENST00000610538.4:c.679G>A	ENSP00000480868.1:p.Gly227Arg
ENST00000610623.4:c.319G>A	ENSP00000477531.1:p.Gly107Arg
ENST00000615910.4:c.763G>A	ENSP00000482903.1:p.Gly255Arg
ENST00000617185.4:c.796G>A	ENSP00000482258.1:p.Gly266Arg
ENST00000618944.4:c.319G>A	ENSP00000481401.1:p.Gly107Arg
ENST00000619186.4:c.319G>A	ENSP00000484375.1:p.Gly107Arg
ENST00000619485.4:c.679G>A	ENSP00000482537.1:p.Gly227Arg
ENST00000620739.4:c.679G>A	ENSP00000481638.1:p.Gly227Arg
ENST00000622645.4:c.679G>A	ENSP00000482222.1:p.Gly227Arg
ENST00000635293.1:c.679G>A	ENSP00000488924.1:p.Gly227Arg
NM_000546.5:c.796G>A , LRG_321t1:c.796G>A	NP_000537.3:p.Gly266Arg
NM_001126112.2:c.796G>A , LRG_321t2:c.796G>A	NP_001119584.1:p.Gly266Arg
NM_001126113.2:c.796G>A , LRG_321t4:c.796G>A	NP_001119585.1:p.Gly266Arg
NM_001126114.2:c.796G>A , LRG_321t3:c.796G>A	NP_001119586.1:p.Gly266Arg
NM_001126115.1:c.400G>A , LRG_321t5:c.400G>A	NP_001119587.1:p.Gly134Arg
NM_001126116.1:c.400G>A , LRG_321t6:c.400G>A	NP_001119588.1:p.Gly134Arg
NM_001126117.1:c.400G>A , LRG_321t7:c.400G>A	NP_001119589.1:p.Gly134Arg
NM_001126118.1:c.679G>A , LRG_321t8:c.679G>A	NP_001119590.1:p.Gly227Arg
NM_001276695.1:c.679G>A	NP_001263624.1:p.Gly227Arg
NM_001276696.1:c.679G>A	NP_001263625.1:p.Gly227Arg
NM_001276697.1:c.319G>A	NP_001263626.1:p.Gly107Arg
NM_001276698.1:c.319G>A	NP_001263627.1:p.Gly107Arg
NM_001276699.1:c.319G>A	NP_001263628.1:p.Gly107Arg
NM_001276760.1:c.679G>A	NP_001263689.1:p.Gly227Arg
NM_001276761.1:c.679G>A	NP_001263690.1:p.Gly227Arg
NM_001276695.2:c.679G>A	NP_001263624.1:p.Gly227Arg
NM_001276696.2:c.679G>A	NP_001263625.1:p.Gly227Arg
NM_001276697.2:c.319G>A	NP_001263626.1:p.Gly107Arg
NM_001276698.2:c.319G>A	NP_001263627.1:p.Gly107Arg
NM_001276699.2:c.319G>A	NP_001263628.1:p.Gly107Arg
NM_001276760.2:c.679G>A	NP_001263689.1:p.Gly227Arg
NM_001276761.2:c.679G>A	NP_001263690.1:p.Gly227Arg
NM_000546.6:c.796G>A MANE Select	NP_000537.3:p.Gly266Arg
NM_001126112.3:c.796G>A	NP_001119584.1:p.Gly266Arg
NM_001126113.3:c.796G>A	NP_001119585.1:p.Gly266Arg
NM_001126114.3:c.796G>A	NP_001119586.1:p.Gly266Arg
NM_001126115.2:c.400G>A	NP_001119587.1:p.Gly134Arg
NM_001126116.2:c.400G>A	NP_001119588.1:p.Gly134Arg
NM_001126117.2:c.400G>A	NP_001119589.1:p.Gly134Arg
NM_001126118.2:c.679G>A	NP_001119590.1:p.Gly227Arg
NM_001276695.3:c.679G>A	NP_001263624.1:p.Gly227Arg
NM_001276696.3:c.679G>A	NP_001263625.1:p.Gly227Arg
NM_001276697.3:c.319G>A	NP_001263626.1:p.Gly107Arg
NM_001276698.3:c.319G>A	NP_001263627.1:p.Gly107Arg
NM_001276699.3:c.319G>A	NP_001263628.1:p.Gly107Arg
NM_001276760.3:c.679G>A	NP_001263689.1:p.Gly227Arg
NM_001276761.3:c.679G>A	NP_001263690.1:p.Gly227Arg