Canonical Allele Identifier: CA645589347

Gene: TP53

Linked Data

• ClinVar Variation Id: 1400022
• ClinVar RCV Id: RCV001917979
• dbSNP Id: rs1064793279
• COSMIC: COSM1480096 ; COSM1480097 ; COSM1480098 ; COSM5229520 ; COSM5229521

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7676118dup , CM000679.2:g.7676118dup	GRCh38
NC_000017.10:g.7579436dup , CM000679.1:g.7579436dup	GRCh37
NC_000017.9:g.7520161dup	NCBI36
NG_017013.2:g.16436dup , LRG_321:g.16436dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000503591.2:c.254dup	ENSP00000426252.2:p.Ala86CysfsTer?
ENST00000508793.6:c.254dup	ENSP00000424104.2:p.Ala86CysfsTer?
ENST00000509690.6:c.-21-879dup	ENSP00000425104.2:n.-21-879dup
ENST00000514944.6:c.96+267dup	ENSP00000423862.2:n.96+267dup
ENST00000604348.6:c.254dup	ENSP00000473895.2:p.Ala86CysfsTer?
ENST00000269305.9:c.254dup MANE Select	ENSP00000269305.4:p.Ala86CysfsTer?
ENST00000269305.8:c.254dup	ENSP00000269305.4:p.Ala86CysfsTer?
ENST00000359597.8:c.254dup	ENSP00000352610.4:p.Ala86CysfsTer?
ENST00000413465.6:c.254dup	ENSP00000410739.2:p.Ala86CysfsTer?
ENST00000420246.6:c.254dup	ENSP00000391127.2:p.Ala86CysfsTer?
ENST00000445888.6:c.254dup	ENSP00000391478.2:p.Ala86CysfsTer?
ENST00000455263.6:c.254dup	ENSP00000398846.2:p.Ala86CysfsTer?
ENST00000503591.1:c.254dup	ENSP00000426252.1:p.Ala86CysfsTer?
ENST00000505014.5:n.510dup
ENST00000508793.5:c.254dup	ENSP00000424104.1:p.Ala86CysfsTer?
ENST00000509690.5:c.-21-879dup	ENSP00000425104.1:n.-21-879dup
ENST00000514944.5:c.96+267dup	ENSP00000423862.1:n.96+267dup
ENST00000604348.5:c.254dup	ENSP00000473895.1:p.Ala86CysfsTer?
ENST00000610292.4:c.137dup	ENSP00000478219.1:p.Ala47CysfsTer?
ENST00000610538.4:c.137dup	ENSP00000480868.1:p.Ala47CysfsTer?
ENST00000615910.4:c.254dup	ENSP00000482903.1:p.Ala86CysfsTer?
ENST00000617185.4:c.254dup	ENSP00000482258.1:p.Ala86CysfsTer?
ENST00000619485.4:c.137dup	ENSP00000482537.1:p.Ala47CysfsTer?
ENST00000620739.4:c.137dup	ENSP00000481638.1:p.Ala47CysfsTer?
ENST00000622645.4:c.137dup	ENSP00000482222.1:p.Ala47CysfsTer?
ENST00000635293.1:c.137dup	ENSP00000488924.1:p.Ala47CysfsTer?
NM_000546.5:c.254dup , LRG_321t1:c.254dup	NP_000537.3:p.Ala86CysfsTer?
NM_001126112.2:c.254dup , LRG_321t2:c.254dup	NP_001119584.1:p.Ala86CysfsTer?
NM_001126113.2:c.254dup , LRG_321t4:c.254dup	NP_001119585.1:p.Ala86CysfsTer?
NM_001126114.2:c.254dup , LRG_321t3:c.254dup	NP_001119586.1:p.Ala86CysfsTer?
NM_001126118.1:c.137dup , LRG_321t8:c.137dup	NP_001119590.1:p.Ala47CysfsTer?
NM_001276695.1:c.137dup	NP_001263624.1:p.Ala47CysfsTer?
NM_001276696.1:c.137dup	NP_001263625.1:p.Ala47CysfsTer?
NM_001276760.1:c.137dup	NP_001263689.1:p.Ala47CysfsTer?
NM_001276761.1:c.137dup	NP_001263690.1:p.Ala47CysfsTer?
NM_001276695.2:c.137dup	NP_001263624.1:p.Ala47CysfsTer?
NM_001276696.2:c.137dup	NP_001263625.1:p.Ala47CysfsTer?
NM_001276760.2:c.137dup	NP_001263689.1:p.Ala47CysfsTer?
NM_001276761.2:c.137dup	NP_001263690.1:p.Ala47CysfsTer?
NM_000546.6:c.254dup MANE Select	NP_000537.3:p.Ala86CysfsTer?
NM_001126112.3:c.254dup	NP_001119584.1:p.Ala86CysfsTer?
NM_001126113.3:c.254dup	NP_001119585.1:p.Ala86CysfsTer?
NM_001126114.3:c.254dup	NP_001119586.1:p.Ala86CysfsTer?
NM_001126118.2:c.137dup	NP_001119590.1:p.Ala47CysfsTer?
NM_001276695.3:c.137dup	NP_001263624.1:p.Ala47CysfsTer?
NM_001276696.3:c.137dup	NP_001263625.1:p.Ala47CysfsTer?
NM_001276760.3:c.137dup	NP_001263689.1:p.Ala47CysfsTer?
NM_001276761.3:c.137dup	NP_001263690.1:p.Ala47CysfsTer?