Canonical Allele Identifier: CA2340621947

Gene: PNKP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861376T= , CM000681.2:g.49861376T=	GRCh38
NC_000019.9:g.50364633T= , CM000681.1:g.50364633T=	GRCh37
NC_000019.8:g.55056445T=	NCBI36
NG_027717.1:g.11190A=
NG_050666.1:g.17533T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1449-11A= MANE Select	ENSP00000323511.2:n.1449-11A=
ENST00000636840.1:c.59+232A=
ENST00000640501.1:c.55-15A=
ENST00000322344.7:c.1449-11A=	ENSP00000323511.2:n.1449-11A=
ENST00000593946.5:c.*1376-11A=	ENSP00000468896.1:n.*1376-11A=
ENST00000594661.5:n.1950-11A=
ENST00000595081.5:n.352-11A=
ENST00000596014.5:c.1449-11A=	ENSP00000472300.1:n.1449-11A=
ENST00000597965.2:c.228A=	ENSP00000471097.2:n.228A=
ENST00000599454.5:n.369-11A=
ENST00000600573.5:c.1356-11A=	ENSP00000469826.1:n.1356-11A=
ENST00000600910.5:c.1339-11A=	ENSP00000473137.1:n.1339-11A=
ENST00000601816.3:n.521-11A=
ENST00000625216.2:c.530-11A=	ENSP00000486898.1:n.530-11A=
ENST00000627232.2:c.1369-11A=	ENSP00000486037.1:n.1369-11A=
ENST00000631020.2:c.1341-11A=	ENSP00000486707.1:n.1341-11A=
NM_007254.3:c.1449-11A=	NP_009185.2:n.1449-11A=
NM_007254.4:c.1449-11A= MANE Select	NP_009185.2:n.1449-11A=