Canonical Allele Identifier: CA2586460344

Gene: PNKP

Linked Data

• gnomAD v4: 19-49861403-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861403A>G , CM000681.2:g.49861403A>G	GRCh38
NC_000019.9:g.50364660A>G , CM000681.1:g.50364660A>G	GRCh37
NC_000019.8:g.55056472A>G	NCBI36
NG_027717.1:g.11163T>C
NG_050666.1:g.17560A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1449-38T>C MANE Select	ENSP00000323511.2:n.1449-38T>C
ENST00000636840.1:c.59+205T>C
ENST00000640501.1:c.55-42T>C
ENST00000322344.7:c.1449-38T>C	ENSP00000323511.2:n.1449-38T>C
ENST00000593946.5:c.*1376-38T>C	ENSP00000468896.1:n.*1376-38T>C
ENST00000594661.5:n.1950-38T>C
ENST00000595081.5:n.352-38T>C
ENST00000596014.5:c.1449-38T>C	ENSP00000472300.1:n.1449-38T>C
ENST00000597965.2:c.201T>C	ENSP00000471097.2:n.201T>C
ENST00000599454.5:n.369-38T>C
ENST00000600573.5:c.1356-38T>C	ENSP00000469826.1:n.1356-38T>C
ENST00000600910.5:c.1339-38T>C	ENSP00000473137.1:n.1339-38T>C
ENST00000601816.3:n.521-38T>C
ENST00000625216.2:c.530-38T>C	ENSP00000486898.1:n.530-38T>C
ENST00000627232.2:c.1369-38T>C	ENSP00000486037.1:n.1369-38T>C
ENST00000631020.2:c.1341-38T>C	ENSP00000486707.1:n.1341-38T>C
NM_007254.3:c.1449-38T>C	NP_009185.2:n.1449-38T>C
NM_007254.4:c.1449-38T>C MANE Select	NP_009185.2:n.1449-38T>C