Canonical Allele Identifier: CA198504
Gene: PNKP HGNC NCBI

Linked Data

ClinVar Variation Id: 187766
ClinVar RCV Id: RCV001813762
dbSNP Id: rs786203983

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49862188C>A , CM000681.2:g.49862188C>A GRCh38
NC_000019.9:g.50365445C>A , CM000681.1:g.50365445C>A GRCh37
NC_000019.8:g.55057257C>A NCBI36
NG_027717.1:g.10378G>T
NG_050666.1:g.18345C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.1123G>T MANE Select ENSP00000323511.2:p.Gly375Trp
ENST00000322344.7:c.1123G>T ENSP00000323511.2:p.Gly375Trp
ENST00000593706.3:n.478G>T
ENST00000593946.5:c.*1050G>T ENSP00000468896.1:n.*1050G>T
ENST00000594661.5:n.1624G>T
ENST00000596014.5:c.1123G>T ENSP00000472300.1:p.Gly375Trp
ENST00000600573.5:c.1030G>T ENSP00000469826.1:p.Gly344Trp
ENST00000600910.5:c.1123G>T ENSP00000473137.1:p.Gly375Trp
ENST00000601816.3:n.22G>T
ENST00000625216.2:c.208-83G>T ENSP00000486898.1:n.208-83G>T
ENST00000627232.2:c.1043G>T ENSP00000486037.1:n.1043G>T
ENST00000627317.1:c.744G>T
ENST00000631020.2:c.1015G>T ENSP00000486707.1:p.Gly339Trp
NM_007254.3:c.1123G>T NP_009185.2:p.Gly375Trp
NM_007254.4:c.1123G>T MANE Select NP_009185.2:p.Gly375Trp