Canonical Allele Identifier: CA406933299

Gene: PNKP

Linked Data

• gnomAD v4: 19-49861693-T-C
• MyVariant Identifiers: chr19:g.50364950T>C (hg19) ; chr19:g.49861693T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861693T>C , CM000681.2:g.49861693T>C	GRCh38
NC_000019.9:g.50364950T>C , CM000681.1:g.50364950T>C	GRCh37
NC_000019.8:g.55056762T>C	NCBI36
NG_027717.1:g.10873A>G
NG_050666.1:g.17850T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1301A>G MANE Select	ENSP00000323511.2:p.Tyr434Cys
ENST00000322344.7:c.1301A>G	ENSP00000323511.2:p.Tyr434Cys
ENST00000593946.5:c.*1228A>G	ENSP00000468896.1:n.*1228A>G
ENST00000594661.5:n.1802A>G
ENST00000595081.5:n.204A>G
ENST00000596014.5:c.1301A>G	ENSP00000472300.1:p.Tyr434Cys
ENST00000597965.2:c.8A>G	ENSP00000471097.2:p.Tyr3Cys
ENST00000599454.5:n.221A>G
ENST00000600573.5:c.1208A>G	ENSP00000469826.1:p.Tyr403Cys
ENST00000600910.5:c.1191A>G	ENSP00000473137.1:p.Val397=
ENST00000601816.3:n.276A>G
ENST00000625216.2:c.382A>G	ENSP00000486898.1:n.382A>G
ENST00000627232.2:c.1221A>G	ENSP00000486037.1:n.1221A>G
ENST00000631020.2:c.1193A>G	ENSP00000486707.1:p.Tyr398Cys
NM_007254.3:c.1301A>G	NP_009185.2:p.Tyr434Cys
NM_007254.4:c.1301A>G MANE Select	NP_009185.2:p.Tyr434Cys