Canonical Allele Identifier: CA2245938189
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668228_7668229delinsCT , CM000679.2:g.7668228_7668229delinsCT GRCh38
NC_000017.10:g.7571546_7571547delinsCT , CM000679.1:g.7571546_7571547delinsCT GRCh37
NC_000017.9:g.7512271_7512272delinsCT NCBI36
NG_017013.2:g.24322_24323delinsAG , LRG_321:g.24322_24323delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1985_994-1984delinsAG ENSP00000352610.4:n.994-1985_994-1984delinsAG
ENST00000413465.6:c.782+5952_782+5953delinsAG ENSP00000410739.2:n.782+5952_782+5953delinsAG
ENST00000635293.1:c.984-804_984-803delinsAG ENSP00000488924.1:n.984-804_984-803delinsAG