Canonical Allele Identifier: CA1677783381

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161973403T= , CM000668.2:g.161973403T=	GRCh38
NC_000006.11:g.162394435T= , CM000668.1:g.162394435T=	GRCh37
NC_000006.10:g.162314425T=	NCBI36
NG_008289.1:g.759400A=
NG_008289.2:g.759400A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004562.3:c.633A= MANE Select	NP_004553.2:p.Lys211=
ENST00000366898.6:c.633A= MANE Select	ENSP00000355865.1:p.Lys211=
NM_004562.2:c.633A=	NP_004553.2:p.Lys211=
NM_013987.2:c.549A=	NP_054642.2:p.Lys183=
NM_013987.3:c.549A=	NP_054642.2:p.Lys183=
NM_013988.2:c.186A=	NP_054643.2:p.Lys62=
NM_013988.3:c.186A=	NP_054643.2:p.Lys62=
ENST00000338468.7:c.60A=	ENSP00000343589.3:p.Lys20=
ENST00000338468.8:c.511A=	ENSP00000343589.4:n.511A=
ENST00000366892.5:c.633A=	ENSP00000355858.1:p.Lys211=
ENST00000366894.5:c.60A=	ENSP00000355860.1:p.Lys20=
ENST00000366894.6:c.392A=	ENSP00000355860.2:n.392A=
ENST00000366896.5:c.186A=	ENSP00000355862.1:p.Lys62=
ENST00000366897.5:c.549A=	ENSP00000355863.1:p.Lys183=
ENST00000366898.5:c.633A=	ENSP00000355865.1:p.Lys211=
ENST00000479615.5:c.396A=	ENSP00000434414.1:p.Lys132=
ENST00000673871.1:c.628A=
ENST00000674232.1:n.651A=
ENST00000674436.1:n.269A=
ENST00000674501.1:n.740A=
XM_011535863.1:c.630A=	XP_011534165.1:p.Lys210=
XM_011535864.1:c.633A=	XP_011534166.1:p.Lys211=
XM_011535865.1:c.633A=	XP_011534167.1:p.Lys211=
XM_011535866.1:c.633A=	XP_011534168.1:p.Lys211=
XM_011535867.1:c.633A=	XP_011534169.1:p.Lys211=
XM_017010908.1:c.747A=	XP_016866397.1:p.Lys249=
XM_017010909.2:c.393A=	XP_016866398.1:p.Lys131=
XM_024446449.1:c.396A=	XP_024302217.1:p.Lys132=
XR_001743443.2:n.739A=