Canonical Allele Identifier: CA406932770

Gene: PNKP

Linked Data

• MyVariant Identifiers: chr19:g.50364727T>G (hg19) ; chr19:g.49861470T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861470T>G , CM000681.2:g.49861470T>G	GRCh38
NC_000019.9:g.50364727T>G , CM000681.1:g.50364727T>G	GRCh37
NC_000019.8:g.55056539T>G	NCBI36
NG_027717.1:g.11096A>C
NG_050666.1:g.17627T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1427A>C MANE Select	ENSP00000323511.2:p.Asp476Ala
ENST00000636840.1:c.59+138A>C
ENST00000640501.1:c.33A>C
ENST00000322344.7:c.1427A>C	ENSP00000323511.2:p.Asp476Ala
ENST00000593946.5:c.*1354A>C	ENSP00000468896.1:n.*1354A>C
ENST00000594661.5:n.1928A>C
ENST00000595081.5:n.330A>C
ENST00000596014.5:c.1427A>C	ENSP00000472300.1:p.Asp476Ala
ENST00000597965.2:c.134A>C	ENSP00000471097.2:p.Asp45Ala
ENST00000599454.5:n.347A>C
ENST00000600573.5:c.1334A>C	ENSP00000469826.1:p.Asp445Ala
ENST00000600910.5:c.1317A>C	ENSP00000473137.1:p.Arg439Ser
ENST00000601816.3:n.499A>C
ENST00000625216.2:c.508A>C	ENSP00000486898.1:n.508A>C
ENST00000627232.2:c.1347A>C	ENSP00000486037.1:n.1347A>C
ENST00000631020.2:c.1319A>C	ENSP00000486707.1:p.Asp440Ala
NM_007254.3:c.1427A>C	NP_009185.2:p.Asp476Ala
NM_007254.4:c.1427A>C MANE Select	NP_009185.2:p.Asp476Ala