Canonical Allele Identifier: CA2340622853
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862408C= , CM000681.2:g.49862408C= GRCh38
NC_000019.9:g.50365665C= , CM000681.1:g.50365665C= GRCh37
NC_000019.8:g.55057477C= NCBI36
NG_027717.1:g.10158G=
NG_050666.1:g.18565C=

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.992G= MANE Select ENSP00000323511.2:p.Trp331=
ENST00000322344.7:c.992G= ENSP00000323511.2:p.Trp331=
ENST00000593706.3:n.347G=
ENST00000593946.5:c.*919G= ENSP00000468896.1:n.*919G=
ENST00000594661.5:n.1493G=
ENST00000596014.5:c.992G= ENSP00000472300.1:p.Trp331=
ENST00000600573.5:c.937-127G= ENSP00000469826.1:n.937-127G=
ENST00000600910.5:c.992G= ENSP00000473137.1:p.Trp331=
ENST00000625216.2:c.170G= ENSP00000486898.1:p.Trp57=
ENST00000627232.2:c.912G= ENSP00000486037.1:n.912G=
ENST00000627317.1:c.613G=
ENST00000629179.1:n.763G=
ENST00000631020.2:c.884G= ENSP00000486707.1:p.Trp295=
NM_007254.3:c.992G= NP_009185.2:p.Trp331=
NM_007254.4:c.992G= MANE Select NP_009185.2:p.Trp331=