Canonical Allele Identifier: CA2340622867
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862424C= , CM000681.2:g.49862424C= GRCh38
NC_000019.9:g.50365681C= , CM000681.1:g.50365681C= GRCh37
NC_000019.8:g.55057493C= NCBI36
NG_027717.1:g.10142G=
NG_050666.1:g.18581C=

Transcript Alleles

HGVS Amino-acid Change
NM_007254.4:c.976G= MANE Select NP_009185.2:p.Glu326=
ENST00000322344.8:c.976G= MANE Select ENSP00000323511.2:p.Glu326=
NM_007254.3:c.976G= NP_009185.2:p.Glu326=
ENST00000322344.7:c.976G= ENSP00000323511.2:p.Glu326=
ENST00000593706.3:n.331G=
ENST00000593946.5:c.*903G= ENSP00000468896.1:n.*903G=
ENST00000594661.5:n.1477G=
ENST00000596014.5:c.976G= ENSP00000472300.1:p.Glu326=
ENST00000600573.5:c.936+114G= ENSP00000469826.1:n.936+114G=
ENST00000600910.5:c.976G= ENSP00000473137.1:p.Glu326=
ENST00000625216.2:c.154G= ENSP00000486898.1:p.Glu52=
ENST00000627232.2:c.896G= ENSP00000486037.1:n.896G=
ENST00000627317.1:c.597G=
ENST00000629179.1:n.747G=
ENST00000631020.2:c.868G= ENSP00000486707.1:p.Glu290=