Canonical Allele Identifier: CA2732929859

Gene: TP53

Linked Data

• dbSNP Id: rs759055064

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7676639G>A , CM000679.2:g.7676639G>A	GRCh38
NC_000017.10:g.7579957G>A , CM000679.1:g.7579957G>A	GRCh37
NC_000017.9:g.7520682G>A	NCBI36
NG_017013.2:g.15912C>T , LRG_321:g.15912C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000503591.2:c.-28-17C>T	ENSP00000426252.2:n.-28-17C>T
ENST00000508793.6:c.-28-17C>T	ENSP00000424104.2:n.-28-17C>T
ENST00000509690.6:c.-21-1403C>T	ENSP00000425104.2:n.-21-1403C>T
ENST00000514944.6:c.-28-17C>T	ENSP00000423862.2:n.-28-17C>T
ENST00000604348.6:c.-28-17C>T	ENSP00000473895.2:n.-28-17C>T
ENST00000269305.9:c.-28-17C>T MANE Select	ENSP00000269305.4:n.-28-17C>T
ENST00000269305.8:c.-28-17C>T	ENSP00000269305.4:n.-28-17C>T
ENST00000420246.6:c.-28-17C>T	ENSP00000391127.2:n.-28-17C>T
ENST00000445888.6:c.-25-20C>T	ENSP00000391478.2:n.-25-20C>T
ENST00000455263.6:c.-28-17C>T	ENSP00000398846.2:n.-28-17C>T
ENST00000503591.1:c.-28-17C>T	ENSP00000426252.1:n.-28-17C>T
ENST00000505014.5:n.112-17C>T
ENST00000508793.5:c.-28-17C>T	ENSP00000424104.1:n.-28-17C>T
ENST00000509690.5:c.-21-1403C>T	ENSP00000425104.1:n.-21-1403C>T
ENST00000514944.5:c.-28-17C>T	ENSP00000423862.1:n.-28-17C>T
ENST00000604348.5:c.-28-17C>T	ENSP00000473895.1:n.-28-17C>T
ENST00000610292.4:c.-262-17C>T	ENSP00000478219.1:n.-262-17C>T
ENST00000610538.4:c.-145-17C>T	ENSP00000480868.1:n.-145-17C>T
ENST00000617185.4:c.-28-17C>T	ENSP00000482258.1:n.-28-17C>T
ENST00000619485.4:c.-142-20C>T	ENSP00000482537.1:n.-142-20C>T
ENST00000620739.4:c.-145-17C>T	ENSP00000481638.1:n.-145-17C>T
ENST00000622645.4:c.-145-17C>T	ENSP00000482222.1:n.-145-17C>T
ENST00000635293.1:c.-145-17C>T	ENSP00000488924.1:n.-145-17C>T
NM_000546.5:c.-28-17C>T , LRG_321t1:c.-28-17C>T	NP_000537.3:n.-28-17C>T
NM_001126112.2:c.-25-20C>T , LRG_321t2:c.-25-20C>T	NP_001119584.1:n.-25-20C>T
NM_001126113.2:c.-28-17C>T , LRG_321t4:c.-28-17C>T	NP_001119585.1:n.-28-17C>T
NM_001126114.2:c.-28-17C>T , LRG_321t3:c.-28-17C>T	NP_001119586.1:n.-28-17C>T
NM_001126118.1:c.-262-17C>T , LRG_321t8:c.-262-17C>T	NP_001119590.1:n.-262-17C>T
NM_001276695.1:c.-145-17C>T	NP_001263624.1:n.-145-17C>T
NM_001276696.1:c.-145-17C>T	NP_001263625.1:n.-145-17C>T
NM_001276760.1:c.-145-17C>T	NP_001263689.1:n.-145-17C>T
NM_001276761.1:c.-142-20C>T	NP_001263690.1:n.-142-20C>T
NM_001276695.2:c.-145-17C>T	NP_001263624.1:n.-145-17C>T
NM_001276696.2:c.-145-17C>T	NP_001263625.1:n.-145-17C>T
NM_001276760.2:c.-145-17C>T	NP_001263689.1:n.-145-17C>T
NM_001276761.2:c.-142-20C>T	NP_001263690.1:n.-142-20C>T
NM_000546.6:c.-28-17C>T MANE Select	NP_000537.3:n.-28-17C>T
NM_001126112.3:c.-25-20C>T	NP_001119584.1:n.-25-20C>T
NM_001126113.3:c.-28-17C>T	NP_001119585.1:n.-28-17C>T
NM_001126114.3:c.-28-17C>T	NP_001119586.1:n.-28-17C>T
NM_001126118.2:c.-262-17C>T	NP_001119590.1:n.-262-17C>T
NM_001276695.3:c.-145-17C>T	NP_001263624.1:n.-145-17C>T
NM_001276696.3:c.-145-17C>T	NP_001263625.1:n.-145-17C>T
NM_001276760.3:c.-145-17C>T	NP_001263689.1:n.-145-17C>T
NM_001276761.3:c.-142-20C>T	NP_001263690.1:n.-142-20C>T