Canonical Allele Identifier: CA2340621972

Gene: PNKP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861416A= , CM000681.2:g.49861416A=	GRCh38
NC_000019.9:g.50364673A= , CM000681.1:g.50364673A=	GRCh37
NC_000019.8:g.55056485A=	NCBI36
NG_027717.1:g.11150T=
NG_050666.1:g.17573A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1448+33T= MANE Select	ENSP00000323511.2:n.1448+33T=
ENST00000636840.1:c.59+192T=
ENST00000640501.1:c.54+33T=
ENST00000322344.7:c.1448+33T=	ENSP00000323511.2:n.1448+33T=
ENST00000593946.5:c.*1375+33T=	ENSP00000468896.1:n.*1375+33T=
ENST00000594661.5:n.1949+33T=
ENST00000595081.5:n.351+33T=
ENST00000596014.5:c.1448+33T=	ENSP00000472300.1:n.1448+33T=
ENST00000597965.2:c.188T=	ENSP00000471097.2:n.188T=
ENST00000599454.5:n.368+33T=
ENST00000600573.5:c.1355+33T=	ENSP00000469826.1:n.1355+33T=
ENST00000600910.5:c.1338+33T=	ENSP00000473137.1:n.1338+33T=
ENST00000601816.3:n.520+33T=
ENST00000625216.2:c.529+33T=	ENSP00000486898.1:n.529+33T=
ENST00000627232.2:c.1368+33T=	ENSP00000486037.1:n.1368+33T=
ENST00000631020.2:c.1340+33T=	ENSP00000486707.1:n.1340+33T=
NM_007254.3:c.1448+33T=	NP_009185.2:n.1448+33T=
NM_007254.4:c.1448+33T= MANE Select	NP_009185.2:n.1448+33T=