Canonical Allele Identifier: CA9586515
Gene: PNKP HGNC NCBI

Linked Data

ClinVar Variation Id: 383110
dbSNP Id: rs372404688

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49861863G>A , CM000681.2:g.49861863G>A GRCh38
NC_000019.9:g.50365120G>A , CM000681.1:g.50365120G>A GRCh37
NC_000019.8:g.55056932G>A NCBI36
NG_027717.1:g.10703C>T
NG_050666.1:g.18020G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000322344.8:c.1207C>T MANE Select ENSP00000323511.2:p.Gln403Ter
ENST00000322344.7:c.1207C>T ENSP00000323511.2:p.Gln403Ter
ENST00000593706.3:n.803C>T
ENST00000593946.5:c.*1134C>T ENSP00000468896.1:n.*1134C>T
ENST00000594661.5:n.1708C>T
ENST00000595081.5:n.34C>T
ENST00000596014.5:c.1207C>T ENSP00000472300.1:p.Gln403Ter
ENST00000599454.5:n.51C>T
ENST00000600573.5:c.1114C>T ENSP00000469826.1:p.Gln372Ter
ENST00000600910.5:c.1189-168C>T ENSP00000473137.1:n.1189-168C>T
ENST00000601816.3:n.106C>T
ENST00000625216.2:c.288C>T ENSP00000486898.1:n.288C>T
ENST00000627232.2:c.1127C>T ENSP00000486037.1:n.1127C>T
ENST00000631020.2:c.1099C>T ENSP00000486707.1:p.Gln367Ter
NM_007254.3:c.1207C>T NP_009185.2:p.Gln403Ter
NM_007254.4:c.1207C>T MANE Select NP_009185.2:p.Gln403Ter