Canonical Allele Identifier: CA2542428706

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443080_162443081insATACCC , CM000668.2:g.162443080_162443081insATACCC	GRCh38
NC_000006.11:g.162864112_162864113insATACCC , CM000668.1:g.162864112_162864113insATACCC	GRCh37
NC_000006.10:g.162784102_162784103insATACCC	NCBI36
NG_008289.1:g.289722_289723insGGGTAT
NG_008289.2:g.289722_289723insGGGTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.171+229_171+230insGGGTAT	ENSP00000343589.4:n.171+229_171+230insGGGTAT
ENST00000366894.6:c.171+229_171+230insGGGTAT	ENSP00000355860.2:n.171+229_171+230insGGGTAT
ENST00000366898.6:c.171+229_171+230insGGGTAT MANE Select	ENSP00000355865.1:n.171+229_171+230insGGGTAT
ENST00000673871.1:c.166+229_166+230insGGGTAT
ENST00000674232.1:n.189+229_189+230insGGGTAT
ENST00000674259.1:n.228+229_228+230insGGGTAT
ENST00000674493.1:n.188+229_188+230insGGGTAT
ENST00000674501.1:n.278+229_278+230insGGGTAT
ENST00000338468.7:c.-281+229_-281+230insGGGTAT	ENSP00000343589.3:n.-281+229_-281+230insGGGTAT
ENST00000366892.5:c.171+229_171+230insGGGTAT	ENSP00000355858.1:n.171+229_171+230insGGGTAT
ENST00000366894.5:c.-162+229_-162+230insGGGTAT	ENSP00000355860.1:n.-162+229_-162+230insGGGTAT
ENST00000366896.5:c.171+229_171+230insGGGTAT	ENSP00000355862.1:n.171+229_171+230insGGGTAT
ENST00000366897.5:c.171+229_171+230insGGGTAT	ENSP00000355863.1:n.171+229_171+230insGGGTAT
ENST00000366898.5:c.171+229_171+230insGGGTAT	ENSP00000355865.1:n.171+229_171+230insGGGTAT
ENST00000479615.5:c.-66-180316_-66-180315insGGGTAT	ENSP00000434414.1:n.-66-180316_-66-180315insGGGTAT
NM_004562.2:c.171+229_171+230insGGGTAT	NP_004553.2:n.171+229_171+230insGGGTAT
NM_013987.2:c.171+229_171+230insGGGTAT	NP_054642.2:n.171+229_171+230insGGGTAT
NM_013988.2:c.171+229_171+230insGGGTAT	NP_054643.2:n.171+229_171+230insGGGTAT
XM_011535863.1:c.171+229_171+230insGGGTAT	XP_011534165.1:n.171+229_171+230insGGGTAT
XM_011535864.1:c.171+229_171+230insGGGTAT	XP_011534166.1:n.171+229_171+230insGGGTAT
XM_011535865.1:c.171+229_171+230insGGGTAT	XP_011534167.1:n.171+229_171+230insGGGTAT
XM_011535866.1:c.171+229_171+230insGGGTAT	XP_011534168.1:n.171+229_171+230insGGGTAT
XM_011535867.1:c.171+229_171+230insGGGTAT	XP_011534169.1:n.171+229_171+230insGGGTAT
XM_017010908.1:c.285+229_285+230insGGGTAT	XP_016866397.1:n.285+229_285+230insGGGTAT
XM_017010909.2:c.-66-180316_-66-180315insGGGTAT	XP_016866398.1:n.-66-180316_-66-180315insGGGTAT
XM_024446449.1:c.-66-180316_-66-180315insGGGTAT	XP_024302217.1:n.-66-180316_-66-180315insGGGTAT
XR_001743443.2:n.277+229_277+230insGGGTAT
NM_004562.3:c.171+229_171+230insGGGTAT MANE Select	NP_004553.2:n.171+229_171+230insGGGTAT
NM_013987.3:c.171+229_171+230insGGGTAT	NP_054642.2:n.171+229_171+230insGGGTAT
NM_013988.3:c.171+229_171+230insGGGTAT	NP_054643.2:n.171+229_171+230insGGGTAT