Canonical Allele Identifier: CA1678012771

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162442926_162442949delinsCTGAGCAGCCTGATTGGGAACAAT , CM000668.2:g.162442926_162442949delinsCTGAGCAGCCTGATTGGGAACAAT	GRCh38
NC_000006.11:g.162863958_162863981delinsCTGAGCAGCCTGATTGGGAACAAT , CM000668.1:g.162863958_162863981delinsCTGAGCAGCCTGATTGGGAACAAT	GRCh37
NC_000006.10:g.162783948_162783971delinsCTGAGCAGCCTGATTGGGAACAAT	NCBI36
NG_008289.1:g.289854_289877delinsATTGTTCCCAATCAGGCTGCTCAG
NG_008289.2:g.289854_289877delinsATTGTTCCCAATCAGGCTGCTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000343589.4:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGC...
ENST00000366894.6:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000355860.2:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGC...
ENST00000366898.6:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG MANE Select	ENSP00000355865.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGC...
ENST00000673871.1:c.166+361_166+384delinsATTGTTCCCAATCAGGCTGCTCAG
ENST00000674232.1:n.189+361_189+384delinsATTGTTCCCAATCAGGCTGCTCAG
ENST00000674259.1:n.228+361_228+384delinsATTGTTCCCAATCAGGCTGCTCAG
ENST00000674493.1:n.188+361_188+384delinsATTGTTCCCAATCAGGCTGCTCAG
ENST00000674501.1:n.278+361_278+384delinsATTGTTCCCAATCAGGCTGCTCAG
ENST00000338468.7:c.-281+361_-281+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000343589.3:n.-281+361_-281+384delinsATTGTTCCCAATCAGGCT...
ENST00000366892.5:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000355858.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGC...
ENST00000366894.5:c.-162+361_-162+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000355860.1:n.-162+361_-162+384delinsATTGTTCCCAATCAGGCT...
ENST00000366896.5:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000355862.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGC...
ENST00000366897.5:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000355863.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGC...
ENST00000366898.5:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000355865.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGC...
ENST00000479615.5:c.-66-180184_-66-180161delinsATTGTTCCCAATCAGGCTGCTCAG	ENSP00000434414.1:n.-66-180184_-66-180161delinsATTGTTCCCAATCA...
NM_004562.2:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	NP_004553.2:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG
NM_013987.2:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	NP_054642.2:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG
NM_013988.2:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	NP_054643.2:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG
XM_011535863.1:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	XP_011534165.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCA...
XM_011535864.1:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	XP_011534166.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCA...
XM_011535865.1:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	XP_011534167.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCA...
XM_011535866.1:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	XP_011534168.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCA...
XM_011535867.1:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	XP_011534169.1:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCA...
XM_017010908.1:c.285+361_285+384delinsATTGTTCCCAATCAGGCTGCTCAG	XP_016866397.1:n.285+361_285+384delinsATTGTTCCCAATCAGGCTGCTCA...
XM_017010909.2:c.-66-180184_-66-180161delinsATTGTTCCCAATCAGGCTGCTCAG	XP_016866398.1:n.-66-180184_-66-180161delinsATTGTTCCCAATCAGGC...
XM_024446449.1:c.-66-180184_-66-180161delinsATTGTTCCCAATCAGGCTGCTCAG	XP_024302217.1:n.-66-180184_-66-180161delinsATTGTTCCCAATCAGGC...
XR_001743443.2:n.277+361_277+384delinsATTGTTCCCAATCAGGCTGCTCAG
NM_004562.3:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG MANE Select	NP_004553.2:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG
NM_013987.3:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	NP_054642.2:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG
NM_013988.3:c.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG	NP_054643.2:n.171+361_171+384delinsATTGTTCCCAATCAGGCTGCTCAG