Canonical Allele Identifier: CA1677459369

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161350145C= , CM000668.2:g.161350145C=	GRCh38
NC_000006.11:g.161771177C= , CM000668.1:g.161771177C=	GRCh37
NC_000006.10:g.161691167C=	NCBI36
NG_008289.1:g.1382658G=
NG_008289.2:g.1382658G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000338468.8:c.1230G=	ENSP00000343589.4:n.1230G=
ENST00000366894.6:c.1111G=	ENSP00000355860.2:n.1111G=
ENST00000366898.6:c.1352G= MANE Select	ENSP00000355865.1:p.Cys451=
ENST00000673871.1:c.1433G=
ENST00000674006.1:n.737G=
ENST00000674436.1:n.988G=
ENST00000338468.7:c.779G=	ENSP00000343589.3:p.Cys260=
ENST00000366894.5:c.779G=	ENSP00000355860.1:p.Cys260=
ENST00000366896.5:c.905G=	ENSP00000355862.1:p.Cys302=
ENST00000366897.5:c.1268G=	ENSP00000355863.1:p.Cys423=
ENST00000366898.5:c.1352G=	ENSP00000355865.1:p.Cys451=
ENST00000479615.5:c.*128G=	ENSP00000434414.1:n.*128G=
ENST00000610470.4:c.485G=	ENSP00000483773.1:p.Cys162=
NM_004562.2:c.1352G=	NP_004553.2:p.Cys451=
NM_013987.2:c.1268G=	NP_054642.2:p.Cys423=
NM_013988.2:c.905G=	NP_054643.2:p.Cys302=
XM_011535863.1:c.1349G=	XP_011534165.1:p.Cys450=
XM_017010908.1:c.1466G=	XP_016866397.1:p.Cys489=
XM_017010909.2:c.1112G=	XP_016866398.1:p.Cys371=
XM_024446449.1:c.1115G=	XP_024302217.1:p.Cys372=
XR_001743443.2:n.1544G=
NM_004562.3:c.1352G= MANE Select	NP_004553.2:p.Cys451=
NM_013987.3:c.1268G=	NP_054642.2:p.Cys423=
NM_013988.3:c.905G=	NP_054643.2:p.Cys302=