Canonical Allele Identifier: CA624725076
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1485498453

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668313_7668349del , CM000679.2:g.7668313_7668349del GRCh38
NC_000017.10:g.7571631_7571667del , CM000679.1:g.7571631_7571667del GRCh37
NC_000017.9:g.7512356_7512392del NCBI36
NG_017013.2:g.24208_24244del , LRG_321:g.24208_24244del

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2099_994-2063del ENSP00000352610.4:n.994-2099_994-2063del
ENST00000413465.6:c.782+5838_782+5874del ENSP00000410739.2:n.782+5838_782+5874del
ENST00000635293.1:c.984-918_984-882del ENSP00000488924.1:n.984-918_984-882del