Canonical Allele Identifier: CA2340622003

Gene: PNKP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861455C= , CM000681.2:g.49861455C=	GRCh38
NC_000019.9:g.50364712C= , CM000681.1:g.50364712C=	GRCh37
NC_000019.8:g.55056524C=	NCBI36
NG_027717.1:g.11111G=
NG_050666.1:g.17612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1442G= MANE Select	ENSP00000323511.2:p.Gly481=
ENST00000636840.1:c.59+153G=
ENST00000640501.1:c.48G=
ENST00000322344.7:c.1442G=	ENSP00000323511.2:p.Gly481=
ENST00000593946.5:c.*1369G=	ENSP00000468896.1:n.*1369G=
ENST00000594661.5:n.1943G=
ENST00000595081.5:n.345G=
ENST00000596014.5:c.1442G=	ENSP00000472300.1:p.Gly481=
ENST00000597965.2:c.149G=	ENSP00000471097.2:p.Gly50=
ENST00000599454.5:n.362G=
ENST00000600573.5:c.1349G=	ENSP00000469826.1:p.Gly450=
ENST00000600910.5:c.1332G=	ENSP00000473137.1:p.Trp444=
ENST00000601816.3:n.514G=
ENST00000625216.2:c.523G=	ENSP00000486898.1:n.523G=
ENST00000627232.2:c.1362G=	ENSP00000486037.1:n.1362G=
ENST00000631020.2:c.1334G=	ENSP00000486707.1:p.Gly445=
NM_007254.3:c.1442G=	NP_009185.2:p.Gly481=
NM_007254.4:c.1442G= MANE Select	NP_009185.2:p.Gly481=