Canonical Allele Identifier: CA1677680095

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161785793C= , CM000668.2:g.161785793C=	GRCh38
NC_000006.11:g.162206825C= , CM000668.1:g.162206825C=	GRCh37
NC_000006.10:g.162126815C=	NCBI36
NG_008289.1:g.947010G=
NG_008289.2:g.947010G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004562.3:c.850G= MANE Select	NP_004553.2:p.Gly284=
ENST00000366898.6:c.850G= MANE Select	ENSP00000355865.1:p.Gly284=
NM_004562.2:c.850G=	NP_004553.2:p.Gly284=
NM_013987.2:c.766G=	NP_054642.2:p.Gly256=
NM_013987.3:c.766G=	NP_054642.2:p.Gly256=
NM_013988.2:c.403G=	NP_054643.2:p.Gly135=
NM_013988.3:c.403G=	NP_054643.2:p.Gly135=
ENST00000338468.7:c.277G=	ENSP00000343589.3:p.Gly93=
ENST00000338468.8:c.728G=	ENSP00000343589.4:n.728G=
ENST00000366892.5:c.850G=	ENSP00000355858.1:p.Gly284=
ENST00000366894.5:c.277G=	ENSP00000355860.1:p.Gly93=
ENST00000366894.6:c.609G=	ENSP00000355860.2:n.609G=
ENST00000366896.5:c.403G=	ENSP00000355862.1:p.Gly135=
ENST00000366897.5:c.766G=	ENSP00000355863.1:p.Gly256=
ENST00000366898.5:c.850G=	ENSP00000355865.1:p.Gly284=
ENST00000479615.5:c.613G=	ENSP00000434414.1:p.Gly205=
ENST00000673871.1:c.845G=
ENST00000674006.1:n.235G=
ENST00000674436.1:n.486G=
ENST00000674501.1:n.957G=
XM_011535863.1:c.847G=	XP_011534165.1:p.Gly283=
XM_011535864.1:c.850G=	XP_011534166.1:p.Gly284=
XM_011535865.1:c.850G=	XP_011534167.1:p.Gly284=
XM_017010908.1:c.964G=	XP_016866397.1:p.Gly322=
XM_017010909.2:c.610G=	XP_016866398.1:p.Gly204=
XM_024446449.1:c.613G=	XP_024302217.1:p.Gly205=
XR_001743443.2:n.956G=