Canonical Allele Identifier: CA2340622861
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862419G= , CM000681.2:g.49862419G= GRCh38
NC_000019.9:g.50365676G= , CM000681.1:g.50365676G= GRCh37
NC_000019.8:g.55057488G= NCBI36
NG_027717.1:g.10147C=
NG_050666.1:g.18576G=

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.981C= MANE Select ENSP00000323511.2:p.Phe327=
ENST00000322344.7:c.981C= ENSP00000323511.2:p.Phe327=
ENST00000593706.3:n.336C=
ENST00000593946.5:c.*908C= ENSP00000468896.1:n.*908C=
ENST00000594661.5:n.1482C=
ENST00000596014.5:c.981C= ENSP00000472300.1:p.Phe327=
ENST00000600573.5:c.936+119C= ENSP00000469826.1:n.936+119C=
ENST00000600910.5:c.981C= ENSP00000473137.1:p.Phe327=
ENST00000625216.2:c.159C= ENSP00000486898.1:p.Phe53=
ENST00000627232.2:c.901C= ENSP00000486037.1:n.901C=
ENST00000627317.1:c.602C=
ENST00000629179.1:n.752C=
ENST00000631020.2:c.873C= ENSP00000486707.1:p.Phe291=
NM_007254.3:c.981C= NP_009185.2:p.Phe327=
NM_007254.4:c.981C= MANE Select NP_009185.2:p.Phe327=