Canonical Allele Identifier: CA406932734

Gene: PNKP

Linked Data

• MyVariant Identifiers: chr19:g.50364717C>G (hg19) ; chr19:g.49861460C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49861460C>G , CM000681.2:g.49861460C>G	GRCh38
NC_000019.9:g.50364717C>G , CM000681.1:g.50364717C>G	GRCh37
NC_000019.8:g.55056529C>G	NCBI36
NG_027717.1:g.11106G>C
NG_050666.1:g.17617C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322344.8:c.1437G>C MANE Select	ENSP00000323511.2:p.Met479Ile
ENST00000636840.1:c.59+148G>C
ENST00000640501.1:c.43G>C
ENST00000322344.7:c.1437G>C	ENSP00000323511.2:p.Met479Ile
ENST00000593946.5:c.*1364G>C	ENSP00000468896.1:n.*1364G>C
ENST00000594661.5:n.1938G>C
ENST00000595081.5:n.340G>C
ENST00000596014.5:c.1437G>C	ENSP00000472300.1:p.Met479Ile
ENST00000597965.2:c.144G>C	ENSP00000471097.2:p.Met48Ile
ENST00000599454.5:n.357G>C
ENST00000600573.5:c.1344G>C	ENSP00000469826.1:p.Met448Ile
ENST00000600910.5:c.1327G>C	ENSP00000473137.1:p.Val443Leu
ENST00000601816.3:n.509G>C
ENST00000625216.2:c.518G>C	ENSP00000486898.1:n.518G>C
ENST00000627232.2:c.1357G>C	ENSP00000486037.1:n.1357G>C
ENST00000631020.2:c.1329G>C	ENSP00000486707.1:p.Met443Ile
NM_007254.3:c.1437G>C	NP_009185.2:p.Met479Ile
NM_007254.4:c.1437G>C MANE Select	NP_009185.2:p.Met479Ile