Canonical Allele Identifier: CA2580094829

Gene: TP53

Linked Data

• ClinVar Variation Id: 2081493
• ClinVar RCV Id: RCV002994332

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7674180_7674185del , CM000679.2:g.7674180_7674185del	GRCh38
NC_000017.10:g.7577498_7577503del , CM000679.1:g.7577498_7577503del	GRCh37
NC_000017.9:g.7518223_7518228del	NCBI36
NG_017013.2:g.18368_18373del , LRG_321:g.18368_18373del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.780_782+3del
ENST00000508793.6:c.780_782+3del
ENST00000509690.6:c.384_386+3del
ENST00000514944.6:c.501_503+3del
ENST00000604348.6:c.759_761+3del
ENST00000269305.9:c.780_782+3del
ENST00000269305.8:c.780_782+3del
ENST00000359597.8:c.780_782+3del
ENST00000413465.6:c.780_782+3del
ENST00000420246.6:c.780_782+3del
ENST00000445888.6:c.780_782+3del
ENST00000455263.6:c.780_782+3del
ENST00000504290.5:c.384_386+3del
ENST00000504937.5:c.384_386+3del
ENST00000509690.5:c.384_386+3del
ENST00000510385.5:c.384_386+3del
ENST00000610292.4:c.663_665+3del
ENST00000610538.4:c.663_665+3del
ENST00000610623.4:c.303_305+3del
ENST00000615910.4:c.747_749+3del
ENST00000617185.4:c.780_782+3del
ENST00000618944.4:c.303_305+3del
ENST00000619186.4:c.303_305+3del
ENST00000619485.4:c.663_665+3del
ENST00000620739.4:c.663_665+3del
ENST00000622645.4:c.663_665+3del
ENST00000635293.1:c.663_665+3del
NM_000546.5:c.780_782+3del , LRG_321t1:c.780_782+3del
NM_001126112.2:c.780_782+3del , LRG_321t2:c.780_782+3del
NM_001126113.2:c.780_782+3del , LRG_321t4:c.780_782+3del
NM_001126114.2:c.780_782+3del , LRG_321t3:c.780_782+3del
NM_001126115.1:c.384_386+3del , LRG_321t5:c.384_386+3del
NM_001126116.1:c.384_386+3del , LRG_321t6:c.384_386+3del
NM_001126117.1:c.384_386+3del , LRG_321t7:c.384_386+3del
NM_001126118.1:c.663_665+3del , LRG_321t8:c.663_665+3del
NM_001276695.1:c.663_665+3del
NM_001276696.1:c.663_665+3del
NM_001276697.1:c.303_305+3del
NM_001276698.1:c.303_305+3del
NM_001276699.1:c.303_305+3del
NM_001276760.1:c.663_665+3del
NM_001276761.1:c.663_665+3del
NM_001276695.2:c.663_665+3del
NM_001276696.2:c.663_665+3del
NM_001276697.2:c.303_305+3del
NM_001276698.2:c.303_305+3del
NM_001276699.2:c.303_305+3del
NM_001276760.2:c.663_665+3del
NM_001276761.2:c.663_665+3del
NM_000546.6:c.780_782+3del
NM_001126112.3:c.780_782+3del
NM_001126113.3:c.780_782+3del
NM_001126114.3:c.780_782+3del
NM_001126115.2:c.384_386+3del
NM_001126116.2:c.384_386+3del
NM_001126117.2:c.384_386+3del
NM_001126118.2:c.663_665+3del
NM_001276695.3:c.663_665+3del
NM_001276696.3:c.663_665+3del
NM_001276697.3:c.303_305+3del
NM_001276698.3:c.303_305+3del
NM_001276699.3:c.303_305+3del
NM_001276760.3:c.663_665+3del
NM_001276761.3:c.663_665+3del