Canonical Allele Identifier: CA2499224945
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1174011
ClinVar RCV Id: RCV001527469

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7669589_7676614del , CM000679.2:g.7669589_7676614del GRCh38
NC_000017.10:g.7572907_7579932del , CM000679.1:g.7572907_7579932del GRCh37
NC_000017.9:g.7513632_7520657del NCBI36
NG_017013.2:g.15938_22963del , LRG_321:g.15938_22963del

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.-19_*21del
ENST00000508793.6:c.-19_*21del
ENST00000509690.6:c.-21-1377_*21del
ENST00000514944.6:c.-19_*21del
ENST00000604348.6:c.-19_*21del
ENST00000269305.9:c.-19_*21del
ENST00000269305.8:c.-19_*21del
ENST00000420246.6:c.-19_*310del
ENST00000445888.6:c.-19_*21del
ENST00000455263.6:c.-19_*222del
ENST00000610292.4:c.-253_*21del
ENST00000610538.4:c.-136_*222del
ENST00000617185.4:c.-19_*310del
ENST00000619485.4:c.-136_*21del
ENST00000620739.4:c.-136_*21del
ENST00000622645.4:c.-136_*310del
ENST00000635293.1:c.-136_983+1021del
NM_000546.5:c.-19_*21del , LRG_321t1:c.-19_*21del
NM_001126112.2:c.-19_*21del , LRG_321t2:c.-19_*21del
NM_001126113.2:c.-19_*222del , LRG_321t4:c.-19_*222del
NM_001126114.2:c.-19_*310del , LRG_321t3:c.-19_*310del
NM_001126118.1:c.-253_*21del , LRG_321t8:c.-253_*21del
NM_001276695.1:c.-136_*222del
NM_001276696.1:c.-136_*310del
NM_001276760.1:c.-136_*21del
NM_001276761.1:c.-136_*21del
NM_001276695.2:c.-136_*222del
NM_001276696.2:c.-136_*310del
NM_001276760.2:c.-136_*21del
NM_001276761.2:c.-136_*21del
NM_000546.6:c.-19_*21del
NM_001126112.3:c.-19_*21del
NM_001126113.3:c.-19_*222del
NM_001126114.3:c.-19_*310del
NM_001126118.2:c.-253_*21del
NM_001276695.3:c.-136_*222del
NM_001276696.3:c.-136_*310del
NM_001276760.3:c.-136_*21del
NM_001276761.3:c.-136_*21del