Canonical Allele Identifier: CA16608665

Gene: TP53

Linked Data

• ClinVar Variation Id: 379471
• ClinVar RCV Id: RCV001527467 ; RCV002374641 ; RCV004022313 ; RCV000433836
• dbSNP Id: rs1057520607
• COSMIC: COSM10856 ; COSM126981 ; COSM2744501 ; COSM3388169
• MyVariant Identifiers: chr17:g.7577058C>A (hg19) ; chr17:g.7673740C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7673740C>A , CM000679.2:g.7673740C>A	GRCh38
NC_000017.10:g.7577058C>A , CM000679.1:g.7577058C>A	GRCh37
NC_000017.9:g.7517783C>A	NCBI36
NG_017013.2:g.18811G>T , LRG_321:g.18811G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.880G>T	ENSP00000426252.2:p.Glu294Ter
ENST00000508793.6:c.880G>T	ENSP00000424104.2:p.Glu294Ter
ENST00000509690.6:c.484G>T	ENSP00000425104.2:p.Glu162Ter
ENST00000514944.6:c.601G>T	ENSP00000423862.2:p.Glu201Ter
ENST00000604348.6:c.859G>T	ENSP00000473895.2:p.Glu287Ter
ENST00000269305.9:c.880G>T MANE Select	ENSP00000269305.4:p.Glu294Ter
ENST00000269305.8:c.880G>T	ENSP00000269305.4:p.Glu294Ter
ENST00000359597.8:c.880G>T	ENSP00000352610.4:p.Glu294Ter
ENST00000413465.6:c.782+441G>T	ENSP00000410739.2:n.782+441G>T
ENST00000420246.6:c.880G>T	ENSP00000391127.2:p.Glu294Ter
ENST00000445888.6:c.880G>T	ENSP00000391478.2:p.Glu294Ter
ENST00000455263.6:c.880G>T	ENSP00000398846.2:p.Glu294Ter
ENST00000504290.5:c.484G>T	ENSP00000484409.1:p.Glu162Ter
ENST00000504937.5:c.484G>T	ENSP00000481179.1:p.Glu162Ter
ENST00000509690.5:c.484G>T	ENSP00000425104.1:p.Glu162Ter
ENST00000510385.5:c.484G>T	ENSP00000478499.1:p.Glu162Ter
ENST00000610292.4:c.763G>T	ENSP00000478219.1:p.Glu255Ter
ENST00000610538.4:c.763G>T	ENSP00000480868.1:p.Glu255Ter
ENST00000610623.4:c.403G>T	ENSP00000477531.1:p.Glu135Ter
ENST00000615910.4:c.847G>T	ENSP00000482903.1:p.Glu283Ter
ENST00000617185.4:c.880G>T	ENSP00000482258.1:p.Glu294Ter
ENST00000618944.4:c.403G>T	ENSP00000481401.1:p.Glu135Ter
ENST00000619186.4:c.403G>T	ENSP00000484375.1:p.Glu135Ter
ENST00000619485.4:c.763G>T	ENSP00000482537.1:p.Glu255Ter
ENST00000620739.4:c.763G>T	ENSP00000481638.1:p.Glu255Ter
ENST00000622645.4:c.763G>T	ENSP00000482222.1:p.Glu255Ter
ENST00000635293.1:c.763G>T	ENSP00000488924.1:p.Glu255Ter
NM_000546.5:c.880G>T , LRG_321t1:c.880G>T	NP_000537.3:p.Glu294Ter
NM_001126112.2:c.880G>T , LRG_321t2:c.880G>T	NP_001119584.1:p.Glu294Ter
NM_001126113.2:c.880G>T , LRG_321t4:c.880G>T	NP_001119585.1:p.Glu294Ter
NM_001126114.2:c.880G>T , LRG_321t3:c.880G>T	NP_001119586.1:p.Glu294Ter
NM_001126115.1:c.484G>T , LRG_321t5:c.484G>T	NP_001119587.1:p.Glu162Ter
NM_001126116.1:c.484G>T , LRG_321t6:c.484G>T	NP_001119588.1:p.Glu162Ter
NM_001126117.1:c.484G>T , LRG_321t7:c.484G>T	NP_001119589.1:p.Glu162Ter
NM_001126118.1:c.763G>T , LRG_321t8:c.763G>T	NP_001119590.1:p.Glu255Ter
NM_001276695.1:c.763G>T	NP_001263624.1:p.Glu255Ter
NM_001276696.1:c.763G>T	NP_001263625.1:p.Glu255Ter
NM_001276697.1:c.403G>T	NP_001263626.1:p.Glu135Ter
NM_001276698.1:c.403G>T	NP_001263627.1:p.Glu135Ter
NM_001276699.1:c.403G>T	NP_001263628.1:p.Glu135Ter
NM_001276760.1:c.763G>T	NP_001263689.1:p.Glu255Ter
NM_001276761.1:c.763G>T	NP_001263690.1:p.Glu255Ter
NM_001276695.2:c.763G>T	NP_001263624.1:p.Glu255Ter
NM_001276696.2:c.763G>T	NP_001263625.1:p.Glu255Ter
NM_001276697.2:c.403G>T	NP_001263626.1:p.Glu135Ter
NM_001276698.2:c.403G>T	NP_001263627.1:p.Glu135Ter
NM_001276699.2:c.403G>T	NP_001263628.1:p.Glu135Ter
NM_001276760.2:c.763G>T	NP_001263689.1:p.Glu255Ter
NM_001276761.2:c.763G>T	NP_001263690.1:p.Glu255Ter
NM_000546.6:c.880G>T MANE Select	NP_000537.3:p.Glu294Ter
NM_001126112.3:c.880G>T	NP_001119584.1:p.Glu294Ter
NM_001126113.3:c.880G>T	NP_001119585.1:p.Glu294Ter
NM_001126114.3:c.880G>T	NP_001119586.1:p.Glu294Ter
NM_001126115.2:c.484G>T	NP_001119587.1:p.Glu162Ter
NM_001126116.2:c.484G>T	NP_001119588.1:p.Glu162Ter
NM_001126117.2:c.484G>T	NP_001119589.1:p.Glu162Ter
NM_001126118.2:c.763G>T	NP_001119590.1:p.Glu255Ter
NM_001276695.3:c.763G>T	NP_001263624.1:p.Glu255Ter
NM_001276696.3:c.763G>T	NP_001263625.1:p.Glu255Ter
NM_001276697.3:c.403G>T	NP_001263626.1:p.Glu135Ter
NM_001276698.3:c.403G>T	NP_001263627.1:p.Glu135Ter
NM_001276699.3:c.403G>T	NP_001263628.1:p.Glu135Ter
NM_001276760.3:c.763G>T	NP_001263689.1:p.Glu255Ter
NM_001276761.3:c.763G>T	NP_001263690.1:p.Glu255Ter