Canonical Allele Identifier: CA406933682

Gene: PNKP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861883T>C , CM000681.2:g.49861883T>C	GRCh38
NC_000019.9:g.50365140T>C , CM000681.1:g.50365140T>C	GRCh37
NC_000019.8:g.55056952T>C	NCBI36
NG_027717.1:g.10683A>G
NG_050666.1:g.18040T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_007254.4:c.1189-2A>G MANE Select	NP_009185.2:n.1189-2A>G
ENST00000322344.8:c.1189-2A>G MANE Select	ENSP00000323511.2:n.1189-2A>G
NM_007254.3:c.1189-2A>G	NP_009185.2:n.1189-2A>G
ENST00000322344.7:c.1189-2A>G	ENSP00000323511.2:n.1189-2A>G
ENST00000593706.3:n.783A>G
ENST00000593946.5:c.*1116-2A>G	ENSP00000468896.1:n.*1116-2A>G
ENST00000594661.5:n.1690-2A>G
ENST00000595081.5:n.14A>G
ENST00000596014.5:c.1189-2A>G	ENSP00000472300.1:n.1189-2A>G
ENST00000599454.5:n.33-2A>G
ENST00000600573.5:c.1096-2A>G	ENSP00000469826.1:n.1096-2A>G
ENST00000600910.5:c.1188+161A>G	ENSP00000473137.1:n.1188+161A>G
ENST00000601816.3:n.88-2A>G
ENST00000625216.2:c.270-2A>G	ENSP00000486898.1:n.270-2A>G
ENST00000627232.2:c.1109-2A>G	ENSP00000486037.1:n.1109-2A>G
ENST00000631020.2:c.1081-2A>G	ENSP00000486707.1:n.1081-2A>G