Canonical Allele Identifier: CA2245936822

Gene: TP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7676377_7676392delinsCTTACCAGAACGTTGT , CM000679.2:g.7676377_7676392delinsCTTACCAGAACGTTGT	GRCh38
NC_000017.10:g.7579695_7579710delinsCTTACCAGAACGTTGT , CM000679.1:g.7579695_7579710delinsCTTACCAGAACGTTGT	GRCh37
NC_000017.9:g.7520420_7520435delinsCTTACCAGAACGTTGT	NCBI36
NG_017013.2:g.16159_16174delinsACAACGTTCTGGTAAG , LRG_321:g.16159_16174delinsACAACGTTCTGGTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000508793.6:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000509690.6:c.-21-1156_-21-1141delinsACAACGTTCTGGTAAG	ENSP00000425104.2:n.-21-1156_-21-1141delinsACAACGTTCTGGTAAG
ENST00000514944.6:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000604348.6:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000269305.9:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000269305.8:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000359597.8:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000413465.6:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000420246.6:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000445888.6:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000455263.6:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000503591.1:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000505014.5:n.342_352+5delinsACAACGTTCTGGTAAG
ENST00000508793.5:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000509690.5:c.-21-1156_-21-1141delinsACAACGTTCTGGTAAG	ENSP00000425104.1:n.-21-1156_-21-1141delinsACAACGTTCTGGTAAG
ENST00000514944.5:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000604348.5:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000610292.4:c.-32_-22+5delinsACAACGTTCTGGTAAG
ENST00000610538.4:c.-32_-22+5delinsACAACGTTCTGGTAAG
ENST00000615910.4:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000617185.4:c.86_96+5delinsACAACGTTCTGGTAAG
ENST00000619485.4:c.-32_-22+5delinsACAACGTTCTGGTAAG
ENST00000620739.4:c.-32_-22+5delinsACAACGTTCTGGTAAG
ENST00000622645.4:c.-32_-22+5delinsACAACGTTCTGGTAAG
ENST00000635293.1:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_000546.5:c.86_96+5delinsACAACGTTCTGGTAAG , LRG_321t1:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126112.2:c.86_96+5delinsACAACGTTCTGGTAAG , LRG_321t2:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126113.2:c.86_96+5delinsACAACGTTCTGGTAAG , LRG_321t4:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126114.2:c.86_96+5delinsACAACGTTCTGGTAAG , LRG_321t3:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126118.1:c.-32_-22+5delinsACAACGTTCTGGTAAG , LRG_321t8:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276695.1:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276696.1:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276760.1:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276761.1:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276695.2:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276696.2:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276760.2:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276761.2:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_000546.6:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126112.3:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126113.3:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126114.3:c.86_96+5delinsACAACGTTCTGGTAAG
NM_001126118.2:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276695.3:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276696.3:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276760.3:c.-32_-22+5delinsACAACGTTCTGGTAAG
NM_001276761.3:c.-32_-22+5delinsACAACGTTCTGGTAAG