Canonical Allele Identifier: CA891844044

Gene: TP53

Linked Data

• ClinVar Variation Id: 579855
• ClinVar RCV Id: RCV000703240
• dbSNP Id: rs1567548832
• MyVariant Identifiers: chr17:g.7577493_7577497del (hg19) ; chr17:g.7674175_7674179del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7674179_7674183del , CM000679.2:g.7674179_7674183del	GRCh38
NC_000017.10:g.7577497_7577501del , CM000679.1:g.7577497_7577501del	GRCh37
NC_000017.9:g.7518222_7518226del	NCBI36
NG_017013.2:g.18372_18376del , LRG_321:g.18372_18376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.782+2_782+6del
ENST00000508793.6:c.782+2_782+6del
ENST00000509690.6:c.386+2_386+6del
ENST00000514944.6:c.503+2_503+6del
ENST00000604348.6:c.761+2_761+6del
ENST00000269305.9:c.782+2_782+6del
ENST00000269305.8:c.782+2_782+6del
ENST00000359597.8:c.782+2_782+6del
ENST00000413465.6:c.782+2_782+6del
ENST00000420246.6:c.782+2_782+6del
ENST00000445888.6:c.782+2_782+6del
ENST00000455263.6:c.782+2_782+6del
ENST00000504290.5:c.386+2_386+6del
ENST00000504937.5:c.386+2_386+6del
ENST00000509690.5:c.386+2_386+6del
ENST00000510385.5:c.386+2_386+6del
ENST00000610292.4:c.665+2_665+6del
ENST00000610538.4:c.665+2_665+6del
ENST00000610623.4:c.305+2_305+6del
ENST00000615910.4:c.749+2_749+6del
ENST00000617185.4:c.782+2_782+6del
ENST00000618944.4:c.305+2_305+6del
ENST00000619186.4:c.305+2_305+6del
ENST00000619485.4:c.665+2_665+6del
ENST00000620739.4:c.665+2_665+6del
ENST00000622645.4:c.665+2_665+6del
ENST00000635293.1:c.665+2_665+6del
NM_000546.5:c.782+2_782+6del , LRG_321t1:c.782+2_782+6del
NM_001126112.2:c.782+2_782+6del , LRG_321t2:c.782+2_782+6del
NM_001126113.2:c.782+2_782+6del , LRG_321t4:c.782+2_782+6del
NM_001126114.2:c.782+2_782+6del , LRG_321t3:c.782+2_782+6del
NM_001126115.1:c.386+2_386+6del , LRG_321t5:c.386+2_386+6del
NM_001126116.1:c.386+2_386+6del , LRG_321t6:c.386+2_386+6del
NM_001126117.1:c.386+2_386+6del , LRG_321t7:c.386+2_386+6del
NM_001126118.1:c.665+2_665+6del , LRG_321t8:c.665+2_665+6del
NM_001276695.1:c.665+2_665+6del
NM_001276696.1:c.665+2_665+6del
NM_001276697.1:c.305+2_305+6del
NM_001276698.1:c.305+2_305+6del
NM_001276699.1:c.305+2_305+6del
NM_001276760.1:c.665+2_665+6del
NM_001276761.1:c.665+2_665+6del
NM_001276695.2:c.665+2_665+6del
NM_001276696.2:c.665+2_665+6del
NM_001276697.2:c.305+2_305+6del
NM_001276698.2:c.305+2_305+6del
NM_001276699.2:c.305+2_305+6del
NM_001276760.2:c.665+2_665+6del
NM_001276761.2:c.665+2_665+6del
NM_000546.6:c.782+2_782+6del
NM_001126112.3:c.782+2_782+6del
NM_001126113.3:c.782+2_782+6del
NM_001126114.3:c.782+2_782+6del
NM_001126115.2:c.386+2_386+6del
NM_001126116.2:c.386+2_386+6del
NM_001126117.2:c.386+2_386+6del
NM_001126118.2:c.665+2_665+6del
NM_001276695.3:c.665+2_665+6del
NM_001276696.3:c.665+2_665+6del
NM_001276697.3:c.305+2_305+6del
NM_001276698.3:c.305+2_305+6del
NM_001276699.3:c.305+2_305+6del
NM_001276760.3:c.665+2_665+6del
NM_001276761.3:c.665+2_665+6del