Canonical Allele Identifier: CA16615710

Gene: TP53

Linked Data

• ClinVar Variation Id: 406569
• ClinVar RCV Id: RCV000458661
• dbSNP Id: rs1555526462
• MyVariant Identifiers: chr17:g.7579291_7579404del (hg19) ; chr17:g.7675973_7676086del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7675973_7676086del , CM000679.2:g.7675973_7676086del	GRCh38
NC_000017.10:g.7579291_7579404del , CM000679.1:g.7579291_7579404del	GRCh37
NC_000017.9:g.7520016_7520129del	NCBI36
NG_017013.2:g.16465_16578del , LRG_321:g.16465_16578del

Transcript Alleles

HGVS	Amino-acid change
ENST00000503591.2:c.283_375+21del
ENST00000508793.6:c.283_375+21del
ENST00000509690.6:c.-21-850_-21-737del	ENSP00000425104.2:n.-21-850_-21-737del
ENST00000514944.6:c.96+296_96+409del	ENSP00000423862.2:n.96+296_96+409del
ENST00000604348.6:c.283_375+21del
ENST00000269305.9:c.283_375+21del
ENST00000269305.8:c.283_375+21del
ENST00000359597.8:c.283_375+21del
ENST00000413465.6:c.283_375+21del
ENST00000420246.6:c.283_375+21del
ENST00000445888.6:c.283_375+21del
ENST00000455263.6:c.283_375+21del
ENST00000503591.1:c.283_375+21del
ENST00000505014.5:n.539_631+21del
ENST00000508793.5:c.283_375+21del
ENST00000509690.5:c.-21-850_-21-737del	ENSP00000425104.1:n.-21-850_-21-737del
ENST00000514944.5:c.96+296_96+409del	ENSP00000423862.1:n.96+296_96+409del
ENST00000604348.5:c.283_375+21del
ENST00000610292.4:c.166_258+21del
ENST00000610538.4:c.166_258+21del
ENST00000615910.4:c.283_340+52del
ENST00000617185.4:c.283_375+21del
ENST00000619485.4:c.166_258+21del
ENST00000620739.4:c.166_258+21del
ENST00000622645.4:c.166_258+21del
ENST00000635293.1:c.166_258+21del
NM_000546.5:c.283_375+21del , LRG_321t1:c.283_375+21del
NM_001126112.2:c.283_375+21del , LRG_321t2:c.283_375+21del
NM_001126113.2:c.283_375+21del , LRG_321t4:c.283_375+21del
NM_001126114.2:c.283_375+21del , LRG_321t3:c.283_375+21del
NM_001126118.1:c.166_258+21del , LRG_321t8:c.166_258+21del
NM_001276695.1:c.166_258+21del
NM_001276696.1:c.166_258+21del
NM_001276760.1:c.166_258+21del
NM_001276761.1:c.166_258+21del
NM_001276695.2:c.166_258+21del
NM_001276696.2:c.166_258+21del
NM_001276760.2:c.166_258+21del
NM_001276761.2:c.166_258+21del
NM_000546.6:c.283_375+21del
NM_001126112.3:c.283_375+21del
NM_001126113.3:c.283_375+21del
NM_001126114.3:c.283_375+21del
NM_001126118.2:c.166_258+21del
NM_001276695.3:c.166_258+21del
NM_001276696.3:c.166_258+21del
NM_001276760.3:c.166_258+21del
NM_001276761.3:c.166_258+21del