Canonical Allele Identifier: CA1677667923

Gene: PRKN

Linked Data

• dbSNP Id: rs1788139390

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161740415del , CM000668.2:g.161740415del	GRCh38
NC_000006.11:g.162161447del , CM000668.1:g.162161447del	GRCh37
NC_000006.10:g.162081437del	NCBI36
NG_008289.1:g.992390del
NG_008289.2:g.992390del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.749+45359del	ENSP00000343589.4:n.749+45359del
ENST00000366894.6:c.630+45359del	ENSP00000355860.2:n.630+45359del
ENST00000366898.6:c.871+45359del MANE Select	ENSP00000355865.1:n.871+45359del
ENST00000673871.1:c.866+45359del
ENST00000674006.1:n.256+45359del
ENST00000674436.1:n.507+45359del
ENST00000674501.1:n.978+45359del
ENST00000338468.7:c.298+45359del	ENSP00000343589.3:n.298+45359del
ENST00000366892.5:c.871+45359del	ENSP00000355858.1:n.871+45359del
ENST00000366894.5:c.298+45359del	ENSP00000355860.1:n.298+45359del
ENST00000366896.5:c.424+45359del	ENSP00000355862.1:n.424+45359del
ENST00000366897.5:c.787+45359del	ENSP00000355863.1:n.787+45359del
ENST00000366898.5:c.871+45359del	ENSP00000355865.1:n.871+45359del
ENST00000479615.5:c.634+45359del	ENSP00000434414.1:n.634+45359del
NM_004562.2:c.871+45359del	NP_004553.2:n.871+45359del
NM_013987.2:c.787+45359del	NP_054642.2:n.787+45359del
NM_013988.2:c.424+45359del	NP_054643.2:n.424+45359del
XM_011535863.1:c.868+45359del	XP_011534165.1:n.868+45359del
XM_011535864.1:c.871+45359del	XP_011534166.1:n.871+45359del
XM_011535865.1:c.871+45359del	XP_011534167.1:n.871+45359del
XM_017010908.1:c.985+45359del	XP_016866397.1:n.985+45359del
XM_017010909.2:c.631+45359del	XP_016866398.1:n.631+45359del
XM_024446449.1:c.634+45359del	XP_024302217.1:n.634+45359del
XR_001743443.2:n.977+45359del
NM_004562.3:c.871+45359del MANE Select	NP_004553.2:n.871+45359del
NM_013987.3:c.787+45359del	NP_054642.2:n.787+45359del
NM_013988.3:c.424+45359del	NP_054643.2:n.424+45359del