Canonical Allele Identifier: CA2773846541

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443614_162443615insCCCCAAACACACCCAACAC , CM000668.2:g.162443614_162443615insCCCCAAACACACCCAACAC	GRCh38
NC_000006.11:g.162864646_162864647insCCCCAAACACACCCAACAC , CM000668.1:g.162864646_162864647insCCCCAAACACACCCAACAC	GRCh37
NC_000006.10:g.162784636_162784637insCCCCAAACACACCCAACAC	NCBI36
NG_008289.1:g.289188_289189insGTGTTGGGTGTGTTTGGGG
NG_008289.2:g.289188_289189insGTGTTGGGTGTGTTTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	ENSP00000343589.4:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
ENST00000366894.6:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	ENSP00000355860.2:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
ENST00000366898.6:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG MANE Select	ENSP00000355865.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
ENST00000648830.1:n.175-142_175-141insGTGTTGGGTGTGTTTGGGG
ENST00000674232.1:n.26-142_26-141insGTGTTGGGTGTGTTTGGGG
ENST00000674259.1:n.65-142_65-141insGTGTTGGGTGTGTTTGGGG
ENST00000674493.1:n.25-142_25-141insGTGTTGGGTGTGTTTGGGG
ENST00000674501.1:n.115-142_115-141insGTGTTGGGTGTGTTTGGGG
ENST00000338468.7:c.-444-142_-444-141insGTGTTGGGTGTGTTTGGGG	ENSP00000343589.3:n.-444-142_-444-141insGTGTTGGGTGTGTTTGGGG
ENST00000366892.5:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	ENSP00000355858.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
ENST00000366894.5:c.-325-142_-325-141insGTGTTGGGTGTGTTTGGGG	ENSP00000355860.1:n.-325-142_-325-141insGTGTTGGGTGTGTTTGGGG
ENST00000366896.5:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	ENSP00000355862.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
ENST00000366897.5:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	ENSP00000355863.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
ENST00000366898.5:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	ENSP00000355865.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
ENST00000479615.5:c.-66-180850_-66-180849insGTGTTGGGTGTGTTTGGGG	ENSP00000434414.1:n.-66-180850_-66-180849insGTGTTGGGTGTGTTTGG...
NM_004562.2:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	NP_004553.2:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
NM_013987.2:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	NP_054642.2:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
NM_013988.2:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	NP_054643.2:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
XM_011535863.1:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	XP_011534165.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
XM_011535864.1:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	XP_011534166.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
XM_011535865.1:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	XP_011534167.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
XM_011535866.1:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	XP_011534168.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
XM_011535867.1:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	XP_011534169.1:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
XM_017010908.1:c.122-142_122-141insGTGTTGGGTGTGTTTGGGG	XP_016866397.1:n.122-142_122-141insGTGTTGGGTGTGTTTGGGG
XM_017010909.2:c.-66-180850_-66-180849insGTGTTGGGTGTGTTTGGGG	XP_016866398.1:n.-66-180850_-66-180849insGTGTTGGGTGTGTTTGGGG
XM_024446449.1:c.-66-180850_-66-180849insGTGTTGGGTGTGTTTGGGG	XP_024302217.1:n.-66-180850_-66-180849insGTGTTGGGTGTGTTTGGGG
XR_001743443.2:n.114-142_114-141insGTGTTGGGTGTGTTTGGGG
NM_004562.3:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG MANE Select	NP_004553.2:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
NM_013987.3:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	NP_054642.2:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG
NM_013988.3:c.8-142_8-141insGTGTTGGGTGTGTTTGGGG	NP_054643.2:n.8-142_8-141insGTGTTGGGTGTGTTTGGGG