Canonical Allele Identifier: CA2012875009
Gene: PARP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804221_3804222delinsCT , CM000674.2:g.3804221_3804222delinsCT GRCh38
NC_000012.11:g.3913387_3913388delinsCT , CM000674.1:g.3913387_3913388delinsCT GRCh37
NC_000012.10:g.3783648_3783649delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2666_*196+2667delinsAG ENSP00000392392.1:n.*196+2666_*196+2667delinsAG