Canonical Allele Identifier: CA2340622662
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862187C= , CM000681.2:g.49862187C= GRCh38
NC_000019.9:g.50365444C= , CM000681.1:g.50365444C= GRCh37
NC_000019.8:g.55057256C= NCBI36
NG_027717.1:g.10379G=
NG_050666.1:g.18344C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322344.8:c.1124G= MANE Select ENSP00000323511.2:p.Gly375=
ENST00000322344.7:c.1124G= ENSP00000323511.2:p.Gly375=
ENST00000593706.3:n.479G=
ENST00000593946.5:c.*1051G= ENSP00000468896.1:n.*1051G=
ENST00000594661.5:n.1625G=
ENST00000596014.5:c.1124G= ENSP00000472300.1:p.Gly375=
ENST00000600573.5:c.1031G= ENSP00000469826.1:p.Gly344=
ENST00000600910.5:c.1124G= ENSP00000473137.1:p.Gly375=
ENST00000601816.3:n.23G=
ENST00000625216.2:c.208-82G= ENSP00000486898.1:n.208-82G=
ENST00000627232.2:c.1044G= ENSP00000486037.1:n.1044G=
ENST00000627317.1:c.745G=
ENST00000631020.2:c.1016G= ENSP00000486707.1:p.Gly339=
NM_007254.3:c.1124G= NP_009185.2:p.Gly375=
NM_007254.4:c.1124G= MANE Select NP_009185.2:p.Gly375=