Canonical Allele Identifier: CA821756389

Gene: PRKN

Linked Data

• dbSNP Id: rs1471895809
• MyVariant Identifiers: chr6:g.162314806_162314808del (hg19) ; chr6:g.161893774_161893776del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161893774_161893776del , CM000668.2:g.161893774_161893776del	GRCh38
NC_000006.11:g.162314806_162314808del , CM000668.1:g.162314806_162314808del	GRCh37
NC_000006.10:g.162234796_162234798del	NCBI36
NG_008289.1:g.839027_839029del
NG_008289.2:g.839027_839029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.612+79526_612+79528del	ENSP00000343589.4:n.612+79526_612+79528del
ENST00000366894.6:c.493+79526_493+79528del	ENSP00000355860.2:n.493+79526_493+79528del
ENST00000366898.6:c.734+79526_734+79528del MANE Select	ENSP00000355865.1:n.734+79526_734+79528del
ENST00000673871.1:c.729+79526_729+79528del
ENST00000674436.1:n.370+79526_370+79528del
ENST00000674501.1:n.841+79526_841+79528del
ENST00000338468.7:c.161+79526_161+79528del	ENSP00000343589.3:n.161+79526_161+79528del
ENST00000366892.5:c.734+79526_734+79528del	ENSP00000355858.1:n.734+79526_734+79528del
ENST00000366894.5:c.161+79526_161+79528del	ENSP00000355860.1:n.161+79526_161+79528del
ENST00000366896.5:c.287+79526_287+79528del	ENSP00000355862.1:n.287+79526_287+79528del
ENST00000366897.5:c.650+79526_650+79528del	ENSP00000355863.1:n.650+79526_650+79528del
ENST00000366898.5:c.734+79526_734+79528del	ENSP00000355865.1:n.734+79526_734+79528del
ENST00000479615.5:c.497+79526_497+79528del	ENSP00000434414.1:n.497+79526_497+79528del
NM_004562.2:c.734+79526_734+79528del	NP_004553.2:n.734+79526_734+79528del
NM_013987.2:c.650+79526_650+79528del	NP_054642.2:n.650+79526_650+79528del
NM_013988.2:c.287+79526_287+79528del	NP_054643.2:n.287+79526_287+79528del
XM_011535863.1:c.731+79526_731+79528del	XP_011534165.1:n.731+79526_731+79528del
XM_011535864.1:c.734+79526_734+79528del	XP_011534166.1:n.734+79526_734+79528del
XM_011535865.1:c.734+79526_734+79528del	XP_011534167.1:n.734+79526_734+79528del
XM_017010908.1:c.848+79526_848+79528del	XP_016866397.1:n.848+79526_848+79528del
XM_017010909.2:c.494+79526_494+79528del	XP_016866398.1:n.494+79526_494+79528del
XM_024446449.1:c.497+79526_497+79528del	XP_024302217.1:n.497+79526_497+79528del
XR_001743443.2:n.840+79526_840+79528del
NM_004562.3:c.734+79526_734+79528del MANE Select	NP_004553.2:n.734+79526_734+79528del
NM_013987.3:c.650+79526_650+79528del	NP_054642.2:n.650+79526_650+79528del
NM_013988.3:c.287+79526_287+79528del	NP_054643.2:n.287+79526_287+79528del