Canonical Allele Identifier: CA2950870447

Gene: TP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7668403A>G , CM000679.2:g.7668403A>G	GRCh38
NC_000017.10:g.7571721A>G , CM000679.1:g.7571721A>G	GRCh37
NC_000017.9:g.7512446A>G	NCBI36
NG_017013.2:g.24148T>C , LRG_321:g.24148T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000546.5:c.*1206T>C , LRG_321t1:c.*1206T>C	NP_000537.3:n.*1206T>C
NM_001126112.2:c.*1206T>C , LRG_321t2:c.*1206T>C	NP_001119584.1:n.*1206T>C
NM_001126113.2:c.*1407T>C , LRG_321t4:c.*1407T>C	NP_001119585.1:n.*1407T>C
NM_001126114.2:c.*1495T>C , LRG_321t3:c.*1495T>C	NP_001119586.1:n.*1495T>C
NM_001126115.1:c.*1206T>C , LRG_321t5:c.*1206T>C	NP_001119587.1:n.*1206T>C
NM_001126116.1:c.*1495T>C , LRG_321t6:c.*1495T>C	NP_001119588.1:n.*1495T>C
NM_001126117.1:c.*1407T>C , LRG_321t7:c.*1407T>C	NP_001119589.1:n.*1407T>C
NM_001126118.1:c.*1206T>C , LRG_321t8:c.*1206T>C	NP_001119590.1:n.*1206T>C
NM_001276695.1:c.*1407T>C	NP_001263624.1:n.*1407T>C
NM_001276695.2:c.*1407T>C	NP_001263624.1:n.*1407T>C
NM_001276696.1:c.*1495T>C	NP_001263625.1:n.*1495T>C
NM_001276696.2:c.*1495T>C	NP_001263625.1:n.*1495T>C
NM_001276697.1:c.*1206T>C	NP_001263626.1:n.*1206T>C
NM_001276697.2:c.*1206T>C	NP_001263626.1:n.*1206T>C
NM_001276698.1:c.*1495T>C	NP_001263627.1:n.*1495T>C
NM_001276698.2:c.*1495T>C	NP_001263627.1:n.*1495T>C
NM_001276699.1:c.*1407T>C	NP_001263628.1:n.*1407T>C
NM_001276699.2:c.*1407T>C	NP_001263628.1:n.*1407T>C
NM_001276760.1:c.*1206T>C	NP_001263689.1:n.*1206T>C
NM_001276760.2:c.*1206T>C	NP_001263689.1:n.*1206T>C
NM_001276761.1:c.*1206T>C	NP_001263690.1:n.*1206T>C
NM_001276761.2:c.*1206T>C	NP_001263690.1:n.*1206T>C
ENST00000269305.8:c.*1206T>C	ENSP00000269305.4:n.*1206T>C
ENST00000359597.8:c.994-2159T>C	ENSP00000352610.4:n.994-2159T>C
ENST00000413465.6:c.782+5778T>C	ENSP00000410739.2:n.782+5778T>C
ENST00000504290.5:c.*1407T>C	ENSP00000484409.1:n.*1407T>C
ENST00000504937.5:c.*1206T>C	ENSP00000481179.1:n.*1206T>C
ENST00000510385.5:c.*1495T>C	ENSP00000478499.1:n.*1495T>C
ENST00000610292.4:c.*1206T>C	ENSP00000478219.1:n.*1206T>C
ENST00000610623.4:c.*1407T>C	ENSP00000477531.1:n.*1407T>C
ENST00000617185.4:c.*1495T>C	ENSP00000482258.1:n.*1495T>C
ENST00000618944.4:c.*1495T>C	ENSP00000481401.1:n.*1495T>C
ENST00000619186.4:c.*1206T>C	ENSP00000484375.1:n.*1206T>C
ENST00000620739.4:c.*1206T>C	ENSP00000481638.1:n.*1206T>C
ENST00000635293.1:c.984-978T>C	ENSP00000488924.1:n.984-978T>C