Canonical Allele Identifier: CA406932853

Gene: PNKP

Linked Data

• MyVariant Identifiers: chr19:g.50364750G>C (hg19) ; chr19:g.49861493G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861493G>C , CM000681.2:g.49861493G>C	GRCh38
NC_000019.9:g.50364750G>C , CM000681.1:g.50364750G>C	GRCh37
NC_000019.8:g.55056562G>C	NCBI36
NG_027717.1:g.11073C>G
NG_050666.1:g.17650G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1404C>G MANE Select	ENSP00000323511.2:p.Asp468Glu
ENST00000636840.1:c.59+115C>G
ENST00000640501.1:c.10C>G
ENST00000322344.7:c.1404C>G	ENSP00000323511.2:p.Asp468Glu
ENST00000593946.5:c.*1331C>G	ENSP00000468896.1:n.*1331C>G
ENST00000594661.5:n.1905C>G
ENST00000595081.5:n.307C>G
ENST00000596014.5:c.1404C>G	ENSP00000472300.1:p.Asp468Glu
ENST00000597965.2:c.111C>G	ENSP00000471097.2:p.Asp37Glu
ENST00000599454.5:n.324C>G
ENST00000600573.5:c.1311C>G	ENSP00000469826.1:p.Asp437Glu
ENST00000600910.5:c.1294C>G	ENSP00000473137.1:p.Leu432Val
ENST00000601816.3:n.476C>G
ENST00000625216.2:c.485C>G	ENSP00000486898.1:n.485C>G
ENST00000627232.2:c.1324C>G	ENSP00000486037.1:n.1324C>G
ENST00000631020.2:c.1296C>G	ENSP00000486707.1:p.Asp432Glu
NM_007254.3:c.1404C>G	NP_009185.2:p.Asp468Glu
NM_007254.4:c.1404C>G MANE Select	NP_009185.2:p.Asp468Glu