Canonical Allele Identifier: CA151519732

Gene: PRKN

Linked Data

• dbSNP Id: rs914143924
• gnomAD v2: 6-162161466-CTT-C
• gnomAD v3: 6-161740434-CTT-C
• gnomAD v4: 6-161740434-CTT-C
• MyVariant Identifiers: chr6:g.162161467_162161468del (hg19) ; chr6:g.161740435_161740436del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161740437_161740438del , CM000668.2:g.161740437_161740438del	GRCh38
NC_000006.11:g.162161469_162161470del , CM000668.1:g.162161469_162161470del	GRCh37
NC_000006.10:g.162081459_162081460del	NCBI36
NG_008289.1:g.992367_992368del
NG_008289.2:g.992367_992368del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.749+45336_749+45337del	ENSP00000343589.4:n.749+45336_749+45337del
ENST00000366894.6:c.630+45336_630+45337del	ENSP00000355860.2:n.630+45336_630+45337del
ENST00000366898.6:c.871+45336_871+45337del MANE Select	ENSP00000355865.1:n.871+45336_871+45337del
ENST00000673871.1:c.866+45336_866+45337del
ENST00000674006.1:n.256+45336_256+45337del
ENST00000674436.1:n.507+45336_507+45337del
ENST00000674501.1:n.978+45336_978+45337del
ENST00000338468.7:c.298+45336_298+45337del	ENSP00000343589.3:n.298+45336_298+45337del
ENST00000366892.5:c.871+45336_871+45337del	ENSP00000355858.1:n.871+45336_871+45337del
ENST00000366894.5:c.298+45336_298+45337del	ENSP00000355860.1:n.298+45336_298+45337del
ENST00000366896.5:c.424+45336_424+45337del	ENSP00000355862.1:n.424+45336_424+45337del
ENST00000366897.5:c.787+45336_787+45337del	ENSP00000355863.1:n.787+45336_787+45337del
ENST00000366898.5:c.871+45336_871+45337del	ENSP00000355865.1:n.871+45336_871+45337del
ENST00000479615.5:c.634+45336_634+45337del	ENSP00000434414.1:n.634+45336_634+45337del
NM_004562.2:c.871+45336_871+45337del	NP_004553.2:n.871+45336_871+45337del
NM_013987.2:c.787+45336_787+45337del	NP_054642.2:n.787+45336_787+45337del
NM_013988.2:c.424+45336_424+45337del	NP_054643.2:n.424+45336_424+45337del
XM_011535863.1:c.868+45336_868+45337del	XP_011534165.1:n.868+45336_868+45337del
XM_011535864.1:c.871+45336_871+45337del	XP_011534166.1:n.871+45336_871+45337del
XM_011535865.1:c.871+45336_871+45337del	XP_011534167.1:n.871+45336_871+45337del
XM_017010908.1:c.985+45336_985+45337del	XP_016866397.1:n.985+45336_985+45337del
XM_017010909.2:c.631+45336_631+45337del	XP_016866398.1:n.631+45336_631+45337del
XM_024446449.1:c.634+45336_634+45337del	XP_024302217.1:n.634+45336_634+45337del
XR_001743443.2:n.977+45336_977+45337del
NM_004562.3:c.871+45336_871+45337del MANE Select	NP_004553.2:n.871+45336_871+45337del
NM_013987.3:c.787+45336_787+45337del	NP_054642.2:n.787+45336_787+45337del
NM_013988.3:c.424+45336_424+45337del	NP_054643.2:n.424+45336_424+45337del