Canonical Allele Identifier: CA406932753

Gene: PNKP

Linked Data

• MyVariant Identifiers: chr19:g.50364722C>G (hg19) ; chr19:g.49861465C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861465C>G , CM000681.2:g.49861465C>G	GRCh38
NC_000019.9:g.50364722C>G , CM000681.1:g.50364722C>G	GRCh37
NC_000019.8:g.55056534C>G	NCBI36
NG_027717.1:g.11101G>C
NG_050666.1:g.17622C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1432G>C MANE Select	ENSP00000323511.2:p.Val478Leu
ENST00000636840.1:c.59+143G>C
ENST00000640501.1:c.38G>C
ENST00000322344.7:c.1432G>C	ENSP00000323511.2:p.Val478Leu
ENST00000593946.5:c.*1359G>C	ENSP00000468896.1:n.*1359G>C
ENST00000594661.5:n.1933G>C
ENST00000595081.5:n.335G>C
ENST00000596014.5:c.1432G>C	ENSP00000472300.1:p.Val478Leu
ENST00000597965.2:c.139G>C	ENSP00000471097.2:p.Val47Leu
ENST00000599454.5:n.352G>C
ENST00000600573.5:c.1339G>C	ENSP00000469826.1:p.Val447Leu
ENST00000600910.5:c.1322G>C	ENSP00000473137.1:p.Gly441Ala
ENST00000601816.3:n.504G>C
ENST00000625216.2:c.513G>C	ENSP00000486898.1:n.513G>C
ENST00000627232.2:c.1352G>C	ENSP00000486037.1:n.1352G>C
ENST00000631020.2:c.1324G>C	ENSP00000486707.1:p.Val442Leu
NM_007254.3:c.1432G>C	NP_009185.2:p.Val478Leu
NM_007254.4:c.1432G>C MANE Select	NP_009185.2:p.Val478Leu