Canonical Allele Identifier: CA1139665126
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 961330
ClinVar RCV Id: RCV001235008

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7674965_7675432del , CM000679.2:g.7674965_7675432del GRCh38
NC_000017.10:g.7578283_7578750del , CM000679.1:g.7578283_7578750del GRCh37
NC_000017.9:g.7519008_7519475del NCBI36
NG_017013.2:g.17119_17586del , LRG_321:g.17119_17586del

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.376-196_566del
ENST00000508793.6:c.376-196_566del
ENST00000509690.6:c.-21-196_170del
ENST00000514944.6:c.97-196_287del
ENST00000604348.6:c.376-217_545del
ENST00000269305.9:c.376-196_566del
ENST00000269305.8:c.376-196_566del
ENST00000359597.8:c.376-196_566del
ENST00000413465.6:c.376-196_566del
ENST00000420246.6:c.376-196_566del
ENST00000445888.6:c.376-196_566del
ENST00000455263.6:c.376-196_566del
ENST00000504290.5:c.-217_170del
ENST00000504937.5:c.-217_170del
ENST00000505014.5:n.632-196_822del
ENST00000509690.5:c.-21-196_170del
ENST00000510385.5:c.-217_170del
ENST00000514944.5:c.97-196_287del
ENST00000610292.4:c.259-196_449del
ENST00000610538.4:c.259-196_449del
ENST00000610623.4:c.-298_89del
ENST00000615910.4:c.341-194_533del
ENST00000617185.4:c.376-196_566del
ENST00000618944.4:c.-298_89del
ENST00000619186.4:c.-298_89del
ENST00000619485.4:c.259-196_449del
ENST00000620739.4:c.259-196_449del
ENST00000622645.4:c.259-196_449del
ENST00000635293.1:c.259-196_449del
NM_000546.5:c.376-196_566del , LRG_321t1:c.376-196_566del
NM_001126112.2:c.376-196_566del , LRG_321t2:c.376-196_566del
NM_001126113.2:c.376-196_566del , LRG_321t4:c.376-196_566del
NM_001126114.2:c.376-196_566del , LRG_321t3:c.376-196_566del
NM_001126115.1:c.-217_170del , LRG_321t5:c.-217_170del
NM_001126116.1:c.-217_170del , LRG_321t6:c.-217_170del
NM_001126117.1:c.-217_170del , LRG_321t7:c.-217_170del
NM_001126118.1:c.259-196_449del , LRG_321t8:c.259-196_449del
NM_001276695.1:c.259-196_449del
NM_001276696.1:c.259-196_449del
NM_001276697.1:c.-298_89del
NM_001276698.1:c.-298_89del
NM_001276699.1:c.-298_89del
NM_001276760.1:c.259-196_449del
NM_001276761.1:c.259-196_449del
NM_001276695.2:c.259-196_449del
NM_001276696.2:c.259-196_449del
NM_001276760.2:c.259-196_449del
NM_001276761.2:c.259-196_449del
NM_000546.6:c.376-196_566del
NM_001126112.3:c.376-196_566del
NM_001126113.3:c.376-196_566del
NM_001126114.3:c.376-196_566del
NM_001126118.2:c.259-196_449del
NM_001276695.3:c.259-196_449del
NM_001276696.3:c.259-196_449del
NM_001276760.3:c.259-196_449del
NM_001276761.3:c.259-196_449del