Canonical Allele Identifier: CA2340622031

Gene: PNKP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861484A= , CM000681.2:g.49861484A=	GRCh38
NC_000019.9:g.50364741A= , CM000681.1:g.50364741A=	GRCh37
NC_000019.8:g.55056553A=	NCBI36
NG_027717.1:g.11082T=
NG_050666.1:g.17641A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1413T= MANE Select	ENSP00000323511.2:p.His471=
ENST00000636840.1:c.59+124T=
ENST00000640501.1:c.19T=
ENST00000322344.7:c.1413T=	ENSP00000323511.2:p.His471=
ENST00000593946.5:c.*1340T=	ENSP00000468896.1:n.*1340T=
ENST00000594661.5:n.1914T=
ENST00000595081.5:n.316T=
ENST00000596014.5:c.1413T=	ENSP00000472300.1:p.His471=
ENST00000597965.2:c.120T=	ENSP00000471097.2:p.His40=
ENST00000599454.5:n.333T=
ENST00000600573.5:c.1320T=	ENSP00000469826.1:p.His440=
ENST00000600910.5:c.1303T=	ENSP00000473137.1:p.Tyr435=
ENST00000601816.3:n.485T=
ENST00000625216.2:c.494T=	ENSP00000486898.1:n.494T=
ENST00000627232.2:c.1333T=	ENSP00000486037.1:n.1333T=
ENST00000631020.2:c.1305T=	ENSP00000486707.1:p.His435=
NM_007254.3:c.1413T=	NP_009185.2:p.His471=
NM_007254.4:c.1413T= MANE Select	NP_009185.2:p.His471=