Canonical Allele Identifier: CA2340622854
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862410C= , CM000681.2:g.49862410C= GRCh38
NC_000019.9:g.50365667C= , CM000681.1:g.50365667C= GRCh37
NC_000019.8:g.55057479C= NCBI36
NG_027717.1:g.10156G=
NG_050666.1:g.18567C=

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.990G= MANE Select ENSP00000323511.2:p.Lys330=
ENST00000322344.7:c.990G= ENSP00000323511.2:p.Lys330=
ENST00000593706.3:n.345G=
ENST00000593946.5:c.*917G= ENSP00000468896.1:n.*917G=
ENST00000594661.5:n.1491G=
ENST00000596014.5:c.990G= ENSP00000472300.1:p.Lys330=
ENST00000600573.5:c.937-129G= ENSP00000469826.1:n.937-129G=
ENST00000600910.5:c.990G= ENSP00000473137.1:p.Lys330=
ENST00000625216.2:c.168G= ENSP00000486898.1:p.Lys56=
ENST00000627232.2:c.910G= ENSP00000486037.1:n.910G=
ENST00000627317.1:c.611G=
ENST00000629179.1:n.761G=
ENST00000631020.2:c.882G= ENSP00000486707.1:p.Lys294=
NM_007254.3:c.990G= NP_009185.2:p.Lys330=
NM_007254.4:c.990G= MANE Select NP_009185.2:p.Lys330=