Canonical Allele Identifier: CA1677668057

Gene: PRKN

Linked Data

• dbSNP Id: rs1788145259

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161740564_161740567dup , CM000668.2:g.161740564_161740567dup	GRCh38
NC_000006.11:g.162161596_162161599dup , CM000668.1:g.162161596_162161599dup	GRCh37
NC_000006.10:g.162081586_162081589dup	NCBI36
NG_008289.1:g.992237_992240dup
NG_008289.2:g.992237_992240dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.749+45206_749+45209dup	ENSP00000343589.4:n.749+45206_749+45209dup
ENST00000366894.6:c.630+45206_630+45209dup	ENSP00000355860.2:n.630+45206_630+45209dup
ENST00000366898.6:c.871+45206_871+45209dup MANE Select	ENSP00000355865.1:n.871+45206_871+45209dup
ENST00000673871.1:c.866+45206_866+45209dup
ENST00000674006.1:n.256+45206_256+45209dup
ENST00000674436.1:n.507+45206_507+45209dup
ENST00000674501.1:n.978+45206_978+45209dup
ENST00000338468.7:c.298+45206_298+45209dup	ENSP00000343589.3:n.298+45206_298+45209dup
ENST00000366892.5:c.871+45206_871+45209dup	ENSP00000355858.1:n.871+45206_871+45209dup
ENST00000366894.5:c.298+45206_298+45209dup	ENSP00000355860.1:n.298+45206_298+45209dup
ENST00000366896.5:c.424+45206_424+45209dup	ENSP00000355862.1:n.424+45206_424+45209dup
ENST00000366897.5:c.787+45206_787+45209dup	ENSP00000355863.1:n.787+45206_787+45209dup
ENST00000366898.5:c.871+45206_871+45209dup	ENSP00000355865.1:n.871+45206_871+45209dup
ENST00000479615.5:c.634+45206_634+45209dup	ENSP00000434414.1:n.634+45206_634+45209dup
NM_004562.2:c.871+45206_871+45209dup	NP_004553.2:n.871+45206_871+45209dup
NM_013987.2:c.787+45206_787+45209dup	NP_054642.2:n.787+45206_787+45209dup
NM_013988.2:c.424+45206_424+45209dup	NP_054643.2:n.424+45206_424+45209dup
XM_011535863.1:c.868+45206_868+45209dup	XP_011534165.1:n.868+45206_868+45209dup
XM_011535864.1:c.871+45206_871+45209dup	XP_011534166.1:n.871+45206_871+45209dup
XM_011535865.1:c.871+45206_871+45209dup	XP_011534167.1:n.871+45206_871+45209dup
XM_017010908.1:c.985+45206_985+45209dup	XP_016866397.1:n.985+45206_985+45209dup
XM_017010909.2:c.631+45206_631+45209dup	XP_016866398.1:n.631+45206_631+45209dup
XM_024446449.1:c.634+45206_634+45209dup	XP_024302217.1:n.634+45206_634+45209dup
XR_001743443.2:n.977+45206_977+45209dup
NM_004562.3:c.871+45206_871+45209dup MANE Select	NP_004553.2:n.871+45206_871+45209dup
NM_013987.3:c.787+45206_787+45209dup	NP_054642.2:n.787+45206_787+45209dup
NM_013988.3:c.424+45206_424+45209dup	NP_054643.2:n.424+45206_424+45209dup