Canonical Allele Identifier: CA2340622858
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862414A= , CM000681.2:g.49862414A= GRCh38
NC_000019.9:g.50365671A= , CM000681.1:g.50365671A= GRCh37
NC_000019.8:g.55057483A= NCBI36
NG_027717.1:g.10152T=
NG_050666.1:g.18571A=

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.986T= MANE Select ENSP00000323511.2:p.Leu329=
ENST00000322344.7:c.986T= ENSP00000323511.2:p.Leu329=
ENST00000593706.3:n.341T=
ENST00000593946.5:c.*913T= ENSP00000468896.1:n.*913T=
ENST00000594661.5:n.1487T=
ENST00000596014.5:c.986T= ENSP00000472300.1:p.Leu329=
ENST00000600573.5:c.936+124T= ENSP00000469826.1:n.936+124T=
ENST00000600910.5:c.986T= ENSP00000473137.1:p.Leu329=
ENST00000625216.2:c.164T= ENSP00000486898.1:p.Leu55=
ENST00000627232.2:c.906T= ENSP00000486037.1:n.906T=
ENST00000627317.1:c.607T=
ENST00000629179.1:n.757T=
ENST00000631020.2:c.878T= ENSP00000486707.1:p.Leu293=
NM_007254.3:c.986T= NP_009185.2:p.Leu329=
NM_007254.4:c.986T= MANE Select NP_009185.2:p.Leu329=