Canonical Allele Identifier: CA2573130640
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1328513
ClinVar RCV Id: RCV001796954

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7674861_7676624dup , CM000679.2:g.7674861_7676624dup GRCh38
NC_000017.10:g.7578179_7579942dup , CM000679.1:g.7578179_7579942dup GRCh37
NC_000017.9:g.7518904_7520667dup NCBI36
NG_017013.2:g.15929_17692dup , LRG_321:g.15929_17692dup

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.-28_672dup
ENST00000508793.6:c.-28_672dup
ENST00000509690.6:c.-21-1386_276dup
ENST00000514944.6:c.-28_393dup
ENST00000604348.6:c.-28_651dup
ENST00000269305.9:c.-28_672dup
ENST00000269305.8:c.-28_672dup
ENST00000420246.6:c.-28_672dup
ENST00000445888.6:c.-25-3_672dup
ENST00000455263.6:c.-28_672dup
ENST00000505014.5:n.112_928dup
ENST00000509690.5:c.-21-1386_276dup
ENST00000514944.5:c.-28_393dup
ENST00000610292.4:c.-262_555dup
ENST00000610538.4:c.-145_555dup
ENST00000617185.4:c.-28_672dup
ENST00000619485.4:c.-142-3_555dup
ENST00000620739.4:c.-145_555dup
ENST00000622645.4:c.-145_555dup
ENST00000635293.1:c.-145_555dup
NM_000546.5:c.-28_672dup , LRG_321t1:c.-28_672dup
NM_001126112.2:c.-25-3_672dup , LRG_321t2:c.-25-3_672dup
NM_001126113.2:c.-28_672dup , LRG_321t4:c.-28_672dup
NM_001126114.2:c.-28_672dup , LRG_321t3:c.-28_672dup
NM_001126118.1:c.-262_555dup , LRG_321t8:c.-262_555dup
NM_001276695.1:c.-145_555dup
NM_001276696.1:c.-145_555dup
NM_001276760.1:c.-145_555dup
NM_001276761.1:c.-142-3_555dup
NM_001276695.2:c.-145_555dup
NM_001276696.2:c.-145_555dup
NM_001276760.2:c.-145_555dup
NM_001276761.2:c.-142-3_555dup
NM_000546.6:c.-28_672dup
NM_001126112.3:c.-25-3_672dup
NM_001126113.3:c.-28_672dup
NM_001126114.3:c.-28_672dup
NM_001126118.2:c.-262_555dup
NM_001276695.3:c.-145_555dup
NM_001276696.3:c.-145_555dup
NM_001276760.3:c.-145_555dup
NM_001276761.3:c.-142-3_555dup