Canonical Allele Identifier: CA1678012802

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443004_162443006delinsAAC , CM000668.2:g.162443004_162443006delinsAAC	GRCh38
NC_000006.11:g.162864036_162864038delinsAAC , CM000668.1:g.162864036_162864038delinsAAC	GRCh37
NC_000006.10:g.162784026_162784028delinsAAC	NCBI36
NG_008289.1:g.289797_289799delinsGTT
NG_008289.2:g.289797_289799delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.171+304_171+306delinsGTT	ENSP00000343589.4:n.171+304_171+306delinsGTT
ENST00000366894.6:c.171+304_171+306delinsGTT	ENSP00000355860.2:n.171+304_171+306delinsGTT
ENST00000366898.6:c.171+304_171+306delinsGTT MANE Select	ENSP00000355865.1:n.171+304_171+306delinsGTT
ENST00000673871.1:c.166+304_166+306delinsGTT
ENST00000674232.1:n.189+304_189+306delinsGTT
ENST00000674259.1:n.228+304_228+306delinsGTT
ENST00000674493.1:n.188+304_188+306delinsGTT
ENST00000674501.1:n.278+304_278+306delinsGTT
ENST00000338468.7:c.-281+304_-281+306delinsGTT	ENSP00000343589.3:n.-281+304_-281+306delinsGTT
ENST00000366892.5:c.171+304_171+306delinsGTT	ENSP00000355858.1:n.171+304_171+306delinsGTT
ENST00000366894.5:c.-162+304_-162+306delinsGTT	ENSP00000355860.1:n.-162+304_-162+306delinsGTT
ENST00000366896.5:c.171+304_171+306delinsGTT	ENSP00000355862.1:n.171+304_171+306delinsGTT
ENST00000366897.5:c.171+304_171+306delinsGTT	ENSP00000355863.1:n.171+304_171+306delinsGTT
ENST00000366898.5:c.171+304_171+306delinsGTT	ENSP00000355865.1:n.171+304_171+306delinsGTT
ENST00000479615.5:c.-66-180241_-66-180239delinsGTT	ENSP00000434414.1:n.-66-180241_-66-180239delinsGTT
NM_004562.2:c.171+304_171+306delinsGTT	NP_004553.2:n.171+304_171+306delinsGTT
NM_013987.2:c.171+304_171+306delinsGTT	NP_054642.2:n.171+304_171+306delinsGTT
NM_013988.2:c.171+304_171+306delinsGTT	NP_054643.2:n.171+304_171+306delinsGTT
XM_011535863.1:c.171+304_171+306delinsGTT	XP_011534165.1:n.171+304_171+306delinsGTT
XM_011535864.1:c.171+304_171+306delinsGTT	XP_011534166.1:n.171+304_171+306delinsGTT
XM_011535865.1:c.171+304_171+306delinsGTT	XP_011534167.1:n.171+304_171+306delinsGTT
XM_011535866.1:c.171+304_171+306delinsGTT	XP_011534168.1:n.171+304_171+306delinsGTT
XM_011535867.1:c.171+304_171+306delinsGTT	XP_011534169.1:n.171+304_171+306delinsGTT
XM_017010908.1:c.285+304_285+306delinsGTT	XP_016866397.1:n.285+304_285+306delinsGTT
XM_017010909.2:c.-66-180241_-66-180239delinsGTT	XP_016866398.1:n.-66-180241_-66-180239delinsGTT
XM_024446449.1:c.-66-180241_-66-180239delinsGTT	XP_024302217.1:n.-66-180241_-66-180239delinsGTT
XR_001743443.2:n.277+304_277+306delinsGTT
NM_004562.3:c.171+304_171+306delinsGTT MANE Select	NP_004553.2:n.171+304_171+306delinsGTT
NM_013987.3:c.171+304_171+306delinsGTT	NP_054642.2:n.171+304_171+306delinsGTT
NM_013988.3:c.171+304_171+306delinsGTT	NP_054643.2:n.171+304_171+306delinsGTT