Canonical Allele Identifier: CA406880980

Gene: PNKP

Linked Data

• gnomAD v4: 19-49862409-A-T
• MyVariant Identifiers: chr19:g.50365666A>T (hg19) ; chr19:g.49862409A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49862409A>T , CM000681.2:g.49862409A>T	GRCh38
NC_000019.9:g.50365666A>T , CM000681.1:g.50365666A>T	GRCh37
NC_000019.8:g.55057478A>T	NCBI36
NG_027717.1:g.10157T>A
NG_050666.1:g.18566A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322344.8:c.991T>A MANE Select	ENSP00000323511.2:p.Trp331Arg
ENST00000322344.7:c.991T>A	ENSP00000323511.2:p.Trp331Arg
ENST00000593706.3:n.346T>A
ENST00000593946.5:c.*918T>A	ENSP00000468896.1:n.*918T>A
ENST00000594661.5:n.1492T>A
ENST00000596014.5:c.991T>A	ENSP00000472300.1:p.Trp331Arg
ENST00000600573.5:c.937-128T>A	ENSP00000469826.1:n.937-128T>A
ENST00000600910.5:c.991T>A	ENSP00000473137.1:p.Trp331Arg
ENST00000625216.2:c.169T>A	ENSP00000486898.1:p.Trp57Arg
ENST00000627232.2:c.911T>A	ENSP00000486037.1:n.911T>A
ENST00000627317.1:c.612T>A
ENST00000629179.1:n.762T>A
ENST00000631020.2:c.883T>A	ENSP00000486707.1:p.Trp295Arg
NM_007254.3:c.991T>A	NP_009185.2:p.Trp331Arg
NM_007254.4:c.991T>A MANE Select	NP_009185.2:p.Trp331Arg