Canonical Allele Identifier: CA2340624085
Community Standard Title: NM_007254.4(PNKP):c.610C= (p.Arg204=)
Gene: PNKP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49864205G= , CM000681.2:g.49864205G= GRCh38
NC_000019.9:g.50367462G= , CM000681.1:g.50367462G= GRCh37
NC_000019.8:g.55059274G= NCBI36
NG_027717.1:g.8361C=

Transcript Alleles

HGVS Amino-acid Change
NM_007254.4:c.610C= MANE Select NP_009185.2:p.Arg204=
ENST00000322344.8:c.610C= MANE Select ENSP00000323511.2:p.Arg204=
NM_007254.3:c.610C= NP_009185.2:p.Arg204=
ENST00000322344.7:c.610C= ENSP00000323511.2:p.Arg204=
ENST00000593946.5:c.*537C= ENSP00000468896.1:n.*537C=
ENST00000594661.5:n.1111C=
ENST00000596014.5:c.610C= ENSP00000472300.1:p.Arg204=
ENST00000599543.3:c.610C= ENSP00000469848.2:p.Arg204=
ENST00000600573.5:c.610C= ENSP00000469826.1:p.Arg204=
ENST00000600910.5:c.610C= ENSP00000473137.1:p.Arg204=
ENST00000627232.2:c.530C= ENSP00000486037.1:n.530C=
ENST00000627317.1:c.258-134C=
ENST00000629179.1:n.381C=
ENST00000631020.2:c.610C= ENSP00000486707.1:p.Arg204=
ENST00000636214.1:c.*147C= ENSP00000489983.1:n.*147C=