Canonical Allele Identifier: CA913190574
Gene: TP53 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7670707_7670738del , CM000679.2:g.7670707_7670738del GRCh38
NC_000017.10:g.7574025_7574056del , CM000679.1:g.7574025_7574056del GRCh37
NC_000017.9:g.7514750_7514781del NCBI36
NG_017013.2:g.21814_21845del , LRG_321:g.21814_21845del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503591.2:c.994-22_1003del
ENST00000508793.6:c.994-22_1003del
ENST00000509690.6:c.598-22_607del
ENST00000514944.6:c.715-22_724del
ENST00000604348.6:c.973-22_982del
ENST00000269305.9:c.994-22_1003del
ENST00000269305.8:c.994-22_1003del
ENST00000359597.8:c.993+2798_993+2829del ENSP00000352610.4:n.993+2798_993+2829del
ENST00000413465.6:c.782+3444_782+3475del ENSP00000410739.2:n.782+3444_782+3475del
ENST00000420246.6:c.*101-22_*110del
ENST00000445888.6:c.994-22_1003del
ENST00000455263.6:c.*13-22_*22del
ENST00000504290.5:c.*13-22_*22del
ENST00000504937.5:c.598-22_607del
ENST00000510385.5:c.*101-22_*110del
ENST00000576024.1:c.54-1047_54-1016del
ENST00000610292.4:c.877-22_886del
ENST00000610538.4:c.*13-22_*22del
ENST00000610623.4:c.*13-22_*22del
ENST00000615910.4:c.961-22_970del
ENST00000617185.4:c.*101-22_*110del
ENST00000618944.4:c.*101-22_*110del
ENST00000619186.4:c.517-22_526del
ENST00000619485.4:c.877-22_886del
ENST00000620739.4:c.877-22_886del
ENST00000622645.4:c.*101-22_*110del
ENST00000635293.1:c.877-22_886del
NM_000546.5:c.994-22_1003del , LRG_321t1:c.994-22_1003del
NM_001126112.2:c.994-22_1003del , LRG_321t2:c.994-22_1003del
NM_001126113.2:c.*13-22_*22del , LRG_321t4:c.*13-22_*22del
NM_001126114.2:c.*101-22_*110del , LRG_321t3:c.*101-22_*110del
NM_001126115.1:c.598-22_607del , LRG_321t5:c.598-22_607del
NM_001126116.1:c.*101-22_*110del , LRG_321t6:c.*101-22_*110del
NM_001126117.1:c.*13-22_*22del , LRG_321t7:c.*13-22_*22del
NM_001126118.1:c.877-22_886del , LRG_321t8:c.877-22_886del
NM_001276695.1:c.*13-22_*22del
NM_001276696.1:c.*101-22_*110del
NM_001276697.1:c.517-22_526del
NM_001276698.1:c.*101-22_*110del
NM_001276699.1:c.*13-22_*22del
NM_001276760.1:c.877-22_886del
NM_001276761.1:c.877-22_886del
NM_001276695.2:c.*13-22_*22del
NM_001276696.2:c.*101-22_*110del
NM_001276697.2:c.517-22_526del
NM_001276698.2:c.*101-22_*110del
NM_001276699.2:c.*13-22_*22del
NM_001276760.2:c.877-22_886del
NM_001276761.2:c.877-22_886del
NM_000546.6:c.994-22_1003del
NM_001126112.3:c.994-22_1003del
NM_001126113.3:c.*13-22_*22del
NM_001126114.3:c.*101-22_*110del
NM_001126115.2:c.598-22_607del
NM_001126116.2:c.*101-22_*110del
NM_001126117.2:c.*13-22_*22del
NM_001126118.2:c.877-22_886del
NM_001276695.3:c.*13-22_*22del
NM_001276696.3:c.*101-22_*110del
NM_001276697.3:c.517-22_526del
NM_001276698.3:c.*101-22_*110del
NM_001276699.3:c.*13-22_*22del
NM_001276760.3:c.877-22_886del
NM_001276761.3:c.877-22_886del