Canonical Allele Identifier: CA775165379
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1452794024

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668309del , CM000679.2:g.7668309del GRCh38
NC_000017.10:g.7571627del , CM000679.1:g.7571627del GRCh37
NC_000017.9:g.7512352del NCBI36
NG_017013.2:g.24247del , LRG_321:g.24247del

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2060del ENSP00000352610.4:n.994-2060del
ENST00000413465.6:c.782+5877del ENSP00000410739.2:n.782+5877del
ENST00000635293.1:c.984-879del ENSP00000488924.1:n.984-879del