Canonical Allele Identifier: CA2340622565
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862045C= , CM000681.2:g.49862045C= GRCh38
NC_000019.9:g.50365302C= , CM000681.1:g.50365302C= GRCh37
NC_000019.8:g.55057114C= NCBI36
NG_027717.1:g.10521G=
NG_050666.1:g.18202C=

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.1187G= MANE Select ENSP00000323511.2:p.Arg396=
ENST00000322344.7:c.1187G= ENSP00000323511.2:p.Arg396=
ENST00000593706.3:n.621G=
ENST00000593946.5:c.*1114G= ENSP00000468896.1:n.*1114G=
ENST00000594661.5:n.1688G=
ENST00000596014.5:c.1187G= ENSP00000472300.1:p.Arg396=
ENST00000599454.5:n.31G=
ENST00000600573.5:c.1094G= ENSP00000469826.1:p.Arg365=
ENST00000600910.5:c.1187G= ENSP00000473137.1:p.Arg396=
ENST00000601816.3:n.86G=
ENST00000625216.2:c.268G= ENSP00000486898.1:n.268G=
ENST00000627232.2:c.1107G= ENSP00000486037.1:n.1107G=
ENST00000631020.2:c.1079G= ENSP00000486707.1:p.Arg360=
NM_007254.3:c.1187G= NP_009185.2:p.Arg396=
NM_007254.4:c.1187G= MANE Select NP_009185.2:p.Arg396=