Canonical Allele Identifier: CA406879421

Gene: PNKP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49862188C>T , CM000681.2:g.49862188C>T	GRCh38
NC_000019.9:g.50365445C>T , CM000681.1:g.50365445C>T	GRCh37
NC_000019.8:g.55057257C>T	NCBI36
NG_027717.1:g.10378G>A
NG_050666.1:g.18345C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007254.4:c.1123G>A MANE Select	NP_009185.2:p.Gly375Arg
ENST00000322344.8:c.1123G>A MANE Select	ENSP00000323511.2:p.Gly375Arg
NM_007254.3:c.1123G>A	NP_009185.2:p.Gly375Arg
ENST00000322344.7:c.1123G>A	ENSP00000323511.2:p.Gly375Arg
ENST00000593706.3:n.478G>A
ENST00000593946.5:c.*1050G>A	ENSP00000468896.1:n.*1050G>A
ENST00000594661.5:n.1624G>A
ENST00000596014.5:c.1123G>A	ENSP00000472300.1:p.Gly375Arg
ENST00000600573.5:c.1030G>A	ENSP00000469826.1:p.Gly344Arg
ENST00000600910.5:c.1123G>A	ENSP00000473137.1:p.Gly375Arg
ENST00000601816.3:n.22G>A
ENST00000625216.2:c.208-83G>A	ENSP00000486898.1:n.208-83G>A
ENST00000627232.2:c.1043G>A	ENSP00000486037.1:n.1043G>A
ENST00000627317.1:c.744G>A
ENST00000631020.2:c.1015G>A	ENSP00000486707.1:p.Gly339Arg