Canonical Allele Identifier: CA1677668125

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161740658_161740659delinsGC , CM000668.2:g.161740658_161740659delinsGC	GRCh38
NC_000006.11:g.162161690_162161691delinsGC , CM000668.1:g.162161690_162161691delinsGC	GRCh37
NC_000006.10:g.162081680_162081681delinsGC	NCBI36
NG_008289.1:g.992144_992145delinsGC
NG_008289.2:g.992144_992145delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.749+45113_749+45114delinsGC	ENSP00000343589.4:n.749+45113_749+45114delinsGC
ENST00000366894.6:c.630+45113_630+45114delinsGC	ENSP00000355860.2:n.630+45113_630+45114delinsGC
ENST00000366898.6:c.871+45113_871+45114delinsGC MANE Select	ENSP00000355865.1:n.871+45113_871+45114delinsGC
ENST00000673871.1:c.866+45113_866+45114delinsGC
ENST00000674006.1:n.256+45113_256+45114delinsGC
ENST00000674436.1:n.507+45113_507+45114delinsGC
ENST00000674501.1:n.978+45113_978+45114delinsGC
ENST00000338468.7:c.298+45113_298+45114delinsGC	ENSP00000343589.3:n.298+45113_298+45114delinsGC
ENST00000366892.5:c.871+45113_871+45114delinsGC	ENSP00000355858.1:n.871+45113_871+45114delinsGC
ENST00000366894.5:c.298+45113_298+45114delinsGC	ENSP00000355860.1:n.298+45113_298+45114delinsGC
ENST00000366896.5:c.424+45113_424+45114delinsGC	ENSP00000355862.1:n.424+45113_424+45114delinsGC
ENST00000366897.5:c.787+45113_787+45114delinsGC	ENSP00000355863.1:n.787+45113_787+45114delinsGC
ENST00000366898.5:c.871+45113_871+45114delinsGC	ENSP00000355865.1:n.871+45113_871+45114delinsGC
ENST00000479615.5:c.634+45113_634+45114delinsGC	ENSP00000434414.1:n.634+45113_634+45114delinsGC
NM_004562.2:c.871+45113_871+45114delinsGC	NP_004553.2:n.871+45113_871+45114delinsGC
NM_013987.2:c.787+45113_787+45114delinsGC	NP_054642.2:n.787+45113_787+45114delinsGC
NM_013988.2:c.424+45113_424+45114delinsGC	NP_054643.2:n.424+45113_424+45114delinsGC
XM_011535863.1:c.868+45113_868+45114delinsGC	XP_011534165.1:n.868+45113_868+45114delinsGC
XM_011535864.1:c.871+45113_871+45114delinsGC	XP_011534166.1:n.871+45113_871+45114delinsGC
XM_011535865.1:c.871+45113_871+45114delinsGC	XP_011534167.1:n.871+45113_871+45114delinsGC
XM_017010908.1:c.985+45113_985+45114delinsGC	XP_016866397.1:n.985+45113_985+45114delinsGC
XM_017010909.2:c.631+45113_631+45114delinsGC	XP_016866398.1:n.631+45113_631+45114delinsGC
XM_024446449.1:c.634+45113_634+45114delinsGC	XP_024302217.1:n.634+45113_634+45114delinsGC
XR_001743443.2:n.977+45113_977+45114delinsGC
NM_004562.3:c.871+45113_871+45114delinsGC MANE Select	NP_004553.2:n.871+45113_871+45114delinsGC
NM_013987.3:c.787+45113_787+45114delinsGC	NP_054642.2:n.787+45113_787+45114delinsGC
NM_013988.3:c.424+45113_424+45114delinsGC	NP_054643.2:n.424+45113_424+45114delinsGC