Canonical Allele Identifier: CA2340622086

Gene: PNKP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861539C= , CM000681.2:g.49861539C=	GRCh38
NC_000019.9:g.50364796C= , CM000681.1:g.50364796C=	GRCh37
NC_000019.8:g.55056608C=	NCBI36
NG_027717.1:g.11027G=
NG_050666.1:g.17696C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1387-29G= MANE Select	ENSP00000323511.2:n.1387-29G=
ENST00000636840.1:c.59+69G=
ENST00000322344.7:c.1387-29G=	ENSP00000323511.2:n.1387-29G=
ENST00000593946.5:c.*1314-29G=	ENSP00000468896.1:n.*1314-29G=
ENST00000594661.5:n.1888-29G=
ENST00000595081.5:n.290-29G=
ENST00000596014.5:c.1387-29G=	ENSP00000472300.1:n.1387-29G=
ENST00000597965.2:c.94-29G=	ENSP00000471097.2:n.94-29G=
ENST00000599454.5:n.307-29G=
ENST00000600573.5:c.1294-29G=	ENSP00000469826.1:n.1294-29G=
ENST00000600910.5:c.1277-29G=	ENSP00000473137.1:n.1277-29G=
ENST00000601816.3:n.430G=
ENST00000625216.2:c.468-29G=	ENSP00000486898.1:n.468-29G=
ENST00000627232.2:c.1307-29G=	ENSP00000486037.1:n.1307-29G=
ENST00000631020.2:c.1279-29G=	ENSP00000486707.1:n.1279-29G=
NM_007254.3:c.1387-29G=	NP_009185.2:n.1387-29G=
NM_007254.4:c.1387-29G= MANE Select	NP_009185.2:n.1387-29G=