Canonical Allele Identifier: CA2576858173
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862313del , CM000681.2:g.49862313del GRCh38
NC_000019.9:g.50365570del , CM000681.1:g.50365570del GRCh37
NC_000019.8:g.55057382del NCBI36
NG_027717.1:g.10254del
NG_050666.1:g.18470del

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.1030-31del MANE Select ENSP00000323511.2:n.1030-31del
ENST00000322344.7:c.1030-31del ENSP00000323511.2:n.1030-31del
ENST00000593706.3:n.385-31del
ENST00000593946.5:c.*957-31del ENSP00000468896.1:n.*957-31del
ENST00000594661.5:n.1531-31del
ENST00000596014.5:c.1030-31del ENSP00000472300.1:n.1030-31del
ENST00000600573.5:c.937-31del ENSP00000469826.1:n.937-31del
ENST00000600910.5:c.1030-31del ENSP00000473137.1:n.1030-31del
ENST00000625216.2:c.207+59del ENSP00000486898.1:n.207+59del
ENST00000627232.2:c.950-31del ENSP00000486037.1:n.950-31del
ENST00000627317.1:c.651-31del
ENST00000629179.1:n.801-31del
ENST00000631020.2:c.922-31del ENSP00000486707.1:n.922-31del
NM_007254.3:c.1030-31del NP_009185.2:n.1030-31del
NM_007254.4:c.1030-31del MANE Select NP_009185.2:n.1030-31del