Canonical Allele Identifier: CA1677591855

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161580404T>G , CM000668.2:g.161580404T>G	GRCh38
NC_000006.11:g.162001436T>G , CM000668.1:g.162001436T>G	GRCh37
NC_000006.10:g.161921426T>G	NCBI36
NG_008289.1:g.1152399A>C
NG_008289.2:g.1152399A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.750-10988A>C	ENSP00000343589.4:n.750-10988A>C
ENST00000366894.6:c.631-10988A>C	ENSP00000355860.2:n.631-10988A>C
ENST00000366898.6:c.872-10988A>C MANE Select	ENSP00000355865.1:n.872-10988A>C
ENST00000673871.1:c.867-10988A>C
ENST00000674006.1:n.257-10988A>C
ENST00000674436.1:n.508-10988A>C
ENST00000674501.1:n.979-10988A>C
ENST00000338468.7:c.299-10988A>C	ENSP00000343589.3:n.299-10988A>C
ENST00000366892.5:c.872-10988A>C	ENSP00000355858.1:n.872-10988A>C
ENST00000366894.5:c.299-10988A>C	ENSP00000355860.1:n.299-10988A>C
ENST00000366896.5:c.425-10988A>C	ENSP00000355862.1:n.425-10988A>C
ENST00000366897.5:c.788-10988A>C	ENSP00000355863.1:n.788-10988A>C
ENST00000366898.5:c.872-10988A>C	ENSP00000355865.1:n.872-10988A>C
ENST00000479615.5:c.635-193527A>C	ENSP00000434414.1:n.635-193527A>C
NM_004562.2:c.872-10988A>C	NP_004553.2:n.872-10988A>C
NM_013987.2:c.788-10988A>C	NP_054642.2:n.788-10988A>C
NM_013988.2:c.425-10988A>C	NP_054643.2:n.425-10988A>C
XM_011535863.1:c.869-10988A>C	XP_011534165.1:n.869-10988A>C
XM_011535864.1:c.872-10988A>C	XP_011534166.1:n.872-10988A>C
XM_011535865.1:c.872-10988A>C	XP_011534167.1:n.872-10988A>C
XM_017010908.1:c.986-10988A>C	XP_016866397.1:n.986-10988A>C
XM_017010909.2:c.632-10988A>C	XP_016866398.1:n.632-10988A>C
XM_024446449.1:c.635-10988A>C	XP_024302217.1:n.635-10988A>C
XR_001743443.2:n.978-10988A>C
NM_004562.3:c.872-10988A>C MANE Select	NP_004553.2:n.872-10988A>C
NM_013987.3:c.788-10988A>C	NP_054642.2:n.788-10988A>C
NM_013988.3:c.425-10988A>C	NP_054643.2:n.425-10988A>C