Canonical Allele Identifier: CA1677667859

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161740320_161740329delinsTCTATATCAA , CM000668.2:g.161740320_161740329delinsTCTATATCAA	GRCh38
NC_000006.11:g.162161352_162161361delinsTCTATATCAA , CM000668.1:g.162161352_162161361delinsTCTATATCAA	GRCh37
NC_000006.10:g.162081342_162081351delinsTCTATATCAA	NCBI36
NG_008289.1:g.992474_992483delinsTTGATATAGA
NG_008289.2:g.992474_992483delinsTTGATATAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.749+45443_749+45452delinsTTGATATAGA	ENSP00000343589.4:n.749+45443_749+45452delinsTTGATATAGA
ENST00000366894.6:c.630+45443_630+45452delinsTTGATATAGA	ENSP00000355860.2:n.630+45443_630+45452delinsTTGATATAGA
ENST00000366898.6:c.871+45443_871+45452delinsTTGATATAGA MANE Select	ENSP00000355865.1:n.871+45443_871+45452delinsTTGATATAGA
ENST00000673871.1:c.866+45443_866+45452delinsTTGATATAGA
ENST00000674006.1:n.256+45443_256+45452delinsTTGATATAGA
ENST00000674436.1:n.507+45443_507+45452delinsTTGATATAGA
ENST00000674501.1:n.978+45443_978+45452delinsTTGATATAGA
ENST00000338468.7:c.298+45443_298+45452delinsTTGATATAGA	ENSP00000343589.3:n.298+45443_298+45452delinsTTGATATAGA
ENST00000366892.5:c.871+45443_871+45452delinsTTGATATAGA	ENSP00000355858.1:n.871+45443_871+45452delinsTTGATATAGA
ENST00000366894.5:c.298+45443_298+45452delinsTTGATATAGA	ENSP00000355860.1:n.298+45443_298+45452delinsTTGATATAGA
ENST00000366896.5:c.424+45443_424+45452delinsTTGATATAGA	ENSP00000355862.1:n.424+45443_424+45452delinsTTGATATAGA
ENST00000366897.5:c.787+45443_787+45452delinsTTGATATAGA	ENSP00000355863.1:n.787+45443_787+45452delinsTTGATATAGA
ENST00000366898.5:c.871+45443_871+45452delinsTTGATATAGA	ENSP00000355865.1:n.871+45443_871+45452delinsTTGATATAGA
ENST00000479615.5:c.634+45443_634+45452delinsTTGATATAGA	ENSP00000434414.1:n.634+45443_634+45452delinsTTGATATAGA
NM_004562.2:c.871+45443_871+45452delinsTTGATATAGA	NP_004553.2:n.871+45443_871+45452delinsTTGATATAGA
NM_013987.2:c.787+45443_787+45452delinsTTGATATAGA	NP_054642.2:n.787+45443_787+45452delinsTTGATATAGA
NM_013988.2:c.424+45443_424+45452delinsTTGATATAGA	NP_054643.2:n.424+45443_424+45452delinsTTGATATAGA
XM_011535863.1:c.868+45443_868+45452delinsTTGATATAGA	XP_011534165.1:n.868+45443_868+45452delinsTTGATATAGA
XM_011535864.1:c.871+45443_871+45452delinsTTGATATAGA	XP_011534166.1:n.871+45443_871+45452delinsTTGATATAGA
XM_011535865.1:c.871+45443_871+45452delinsTTGATATAGA	XP_011534167.1:n.871+45443_871+45452delinsTTGATATAGA
XM_017010908.1:c.985+45443_985+45452delinsTTGATATAGA	XP_016866397.1:n.985+45443_985+45452delinsTTGATATAGA
XM_017010909.2:c.631+45443_631+45452delinsTTGATATAGA	XP_016866398.1:n.631+45443_631+45452delinsTTGATATAGA
XM_024446449.1:c.634+45443_634+45452delinsTTGATATAGA	XP_024302217.1:n.634+45443_634+45452delinsTTGATATAGA
XR_001743443.2:n.977+45443_977+45452delinsTTGATATAGA
NM_004562.3:c.871+45443_871+45452delinsTTGATATAGA MANE Select	NP_004553.2:n.871+45443_871+45452delinsTTGATATAGA
NM_013987.3:c.787+45443_787+45452delinsTTGATATAGA	NP_054642.2:n.787+45443_787+45452delinsTTGATATAGA
NM_013988.3:c.424+45443_424+45452delinsTTGATATAGA	NP_054643.2:n.424+45443_424+45452delinsTTGATATAGA