Canonical Allele Identifier: CA2340622500

Gene: PNKP

Linked Data

• dbSNP Id: rs2074772164
• gnomAD v4: 19-49861957-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861957A>G , CM000681.2:g.49861957A>G	GRCh38
NC_000019.9:g.50365214A>G , CM000681.1:g.50365214A>G	GRCh37
NC_000019.8:g.55057026A>G	NCBI36
NG_027717.1:g.10609T>C
NG_050666.1:g.18114A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322344.8:c.1189-76T>C MANE Select	ENSP00000323511.2:n.1189-76T>C
ENST00000322344.7:c.1189-76T>C	ENSP00000323511.2:n.1189-76T>C
ENST00000593706.3:n.709T>C
ENST00000593946.5:c.*1116-76T>C	ENSP00000468896.1:n.*1116-76T>C
ENST00000594661.5:n.1690-76T>C
ENST00000596014.5:c.1189-76T>C	ENSP00000472300.1:n.1189-76T>C
ENST00000599454.5:n.33-76T>C
ENST00000600573.5:c.1096-76T>C	ENSP00000469826.1:n.1096-76T>C
ENST00000600910.5:c.1188+87T>C	ENSP00000473137.1:n.1188+87T>C
ENST00000601816.3:n.88-76T>C
ENST00000625216.2:c.270-76T>C	ENSP00000486898.1:n.270-76T>C
ENST00000627232.2:c.1109-76T>C	ENSP00000486037.1:n.1109-76T>C
ENST00000631020.2:c.1081-76T>C	ENSP00000486707.1:n.1081-76T>C
NM_007254.3:c.1189-76T>C	NP_009185.2:n.1189-76T>C
NM_007254.4:c.1189-76T>C MANE Select	NP_009185.2:n.1189-76T>C