Canonical Allele Identifier: CA2012875030
Gene: PARP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804269_3804272delinsAATC , CM000674.2:g.3804269_3804272delinsAATC GRCh38
NC_000012.11:g.3913435_3913438delinsAATC , CM000674.1:g.3913435_3913438delinsAATC GRCh37
NC_000012.10:g.3783696_3783699delinsAATC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2616_*196+2619delinsGATT ENSP00000392392.1:n.*196+2616_*196+2619delinsGATT